2017-04-28 20:23:19 UPDATED: (M6.8) MINDANAO, PHILIPPINES 5.5 125.1 (442af)

M6.8 - MINDANAO, PHILIPPINES

Preliminary Earthquake Report

Magnitude	6.8
Date-Time	28 Apr 2017 20:23:20 UTC 29 Apr 2017 04:23:20 near epicenter 28 Apr 2017 10:23:20 standard time in your timezone
Location	5.477N 125.084E
Depth	41 km
Distances	72 km (45 miles) S (189 degrees) of General Santos, Mindanao, Philippines 189 km (117 miles) SSW (199 degrees) of Davao, Mindanao, Philippines 216 km (134 miles) SSE (155 degrees) of Cotabato, Mindanao, Philippines 1063 km (660 miles) W (259 degrees) of KOROR, Palau
Location Uncertainty	Horizontal: 7.0 km; Vertical 6.1 km
Parameters	Nph = 101; Dmin = 184.3 km; Rmss = 1.37 seconds; Gp = 31° Version =
Event ID	us 10008ls4

For updates, maps, and technical information
see: Event Page or USGS Earthquake Hazards Program
National Earthquake Information Center
U.S. Geological Survey


Disclaimer

This email was sent to filter@clubhouseb.com

You requested mail for events between -90.0/90.0 latitude and 180.0/-180.0 longitude (Default World)
for M6.0 between 09:00 and 21:00 and M6.5 other times.
Your account has aftershock exclusion turned on. This event fell into the 'AT00op4zax' exclusion region, but was large enough to trigger notification.
To change your parameters, go to: https://earthquake.usgs.gov/ens
To unsubscribe, send a one-line reply to this message with: STOP filter@clubhouseb.com

Phoenix Food, LLC Announces Voluntary Recall Of Dip Trio Mix Due To Possible Health Risk

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Phoenix Food, LLC Announces Voluntary Recall Of Dip Trio Mix Due To Possible Health Risk

04/27/2017 03:09 PM EDT

Phoenix Food, LLC (the company) of Canton, Texas announced it is voluntarily recalling select Dip Trio Mixes due to the potential presence of Salmonella in the seasoning packet. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Lords Organics Recalls Ginger Powder Because Of Possible Health Risk

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Lords Organics Recalls Ginger Powder Because Of Possible Health Risk

04/27/2017 04:45 PM EDT

LORDS ORGANICS is recalling Ginger Powder Product from AGF Organic Veda, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Urban Remedy Issues Voluntary Recall of Mislabeled Non-Dairy Spiced Golden Milk Due to Undeclared Allergen

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Urban Remedy Issues Voluntary Recall of Mislabeled Non-Dairy Spiced Golden Milk Due to Undeclared Allergen

04/28/2017 08:07 AM EDT

Urban Remedy is voluntarily recalling Non-Dairy Spiced Golden Milk that was mislabeled as cold pressed apple juice. The products were sold in select Whole Foods Market stores in Arizona, California and Nevada and contained tree nut (cashew) allergens that were not listed on the product labels. People who have an allergy or severe sensitivity to tree nuts run the risk of serious or life-threatening allergic reaction if they consume these products.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

News from CPSC: 2 Recalls Announced April 26, 2017

 

-----------NEWS from CPSC-----------
U.S. Consumer Product Safety Commission
Office of Communications
4330 East West Highway, Bethesda, MD 20814
www.cpsc.gov

1. Women’s Sweaters Recalled by FatFace Due to Violation of Federal Flammability Standard:

https://cpsc.gov/Recalls/2017/Womens-Sweaters-Recalled-by-FatFace

 

2. Chromag Bicycle Stems Recalled by Riser Holdings Due to Fall and Injury Hazards:

https://www.cpsc.gov/Recalls/2017/Chromag-Bicycle-Stems-Recalled-by-Riser-Holdings/

*********************************************************************************

1. Recall Date: April 26, 2017

Recall Number: 17-141                                                                                                                  

Women’s Sweaters Recalled by FatFace Due to Violation of Federal Flammability Standard

 

Recall Summary

 

Name of Product: Women’s overhead and zip-up sweaters

 

Hazard: The recalled women’s sweaters fail to meet federal flammability standards for clothing textiles, posing a risk of burn injuries.

 

Remedy: Refund

Consumers should immediately stop using the recalled sweaters and contact the firm for instructions on returning the sweaters for a $75 refund.

 

Consumer Contact: FatFace at 800-585-0178 from 4 a.m. to 12:30 p.m. ET Monday through Friday, 5 a.m. to 1 p.m. ET Saturday and 6 a.m. to 12 p.m. ET on Sunday, email at usproductqueries@fatface.com with “Product Recall” as the email subject or online at http://us.fatface.com and click on the “Important Notice” tab for more information. 

 

Photos available here https://cpsc.gov/Recalls/2017/Womens-Sweaters-Recalled-by-FatFace

 

Recall Details

 

Units: About 400

 

Description: This recall involves two styles of FatFace women’s sweaters: overhead Cowes (style number 918043) and zip-up (style number 918041). The style numbers are printed on a care label on the inside seam of the sweaters. 

 

The Overhead Cowes sweater is 97 percent cotton and 3 percent polyester sold in ivory. This sweater has a 3.5 inch cowl or funnel neckline that can be tightened or loosened by the drawstring located at the center front of the neckline. These sweaters also have a kangaroo-style pocket located at the bottom front of the sweater.     

 

The zip-up sweater is 97 percent cotton and 3 percent polyester with a Yarmouth textured zip-up sweater. It sold in ivory, ocean surf (green) and lilac ice (lavender) colors. The sweater has a hood that can be tightened and loosened with a drawstring. The sweater has a silver metal zipper extending from the neckline to the bottom of the sweaters with two pockets on each side of the zipper.   

 

Incidents/Injuries: The firm has received one report of a burn injury.

 

Sold exclusively at: FatFace stores in Maine, Massachusetts and Rhode Island and online at www.fatface.com

from September 2016 through January 2017 for about $60. 

 

Importer: FatFace Corp., of Wilmington, Del.

 

Manufactured in: China

******************************************************************************

2. Recall Date: April 26, 2017

Recall Number: 17-140                                                  

Chromag Bicycle Stems Recalled by Riser Holdings Due to Fall and Injury Hazards

 

Recall Summary

 

Name of Product: Chromag bicycle stems

 

Hazard: The clamping bolts that secure the stem to the fork steerer and/or the handlebars can break, posing fall and injury hazards to riders.

 

Remedy:  Replace

 

Consumer Contact: Chromag Bikes at 800-380-4102 from 9 a.m. to 5 p.m. PT Monday through Thursday, email info@chromagbikes.com or online at www.chromagbikes.com and click on Stem Bolt Recall at the top of the page for more information.

 

Photos available at https://www.cpsc.gov/Recalls/2017/Chromag-Bicycle-Stems-Recalled-by-Riser-Holdings/

 

Recall Details

 

Units: About 100

 

Description: This recall involves Chromag bicycle stems used to clamp the fork steerer and/or handlebars. The recalled stems include models BZA, Director, HiFi and Ranger. Only stems  with a “Z” marked inside the bolt head are included in this recall. “Chromag” and the model name are printed on the stems.  The stems were sold separately from bicycles. Bolts used in the stems are 6 mm in diameter and 20 mm in length. The stems were sold in various colors including black, red, blue, gold, purple and silver.

 

Incidents/Injuries: The firm has received three reports of the clamping bolts breaking. No injuries have been reported.

 

Remedy: Consumers should immediately stop using bicycles with the recalled stems and contact Chromag for free replacement bolts for the stem.

 

Sold at: Arts Cyclery, Beatchwood Cycles, Beat Cycles, Breadwinner Cycles, Blazin Saddles, Harpers, Quality Bicycle Products, The Bike Hub and Squatch Cycles nationwide or online at  www.chromagbikes.com from November 2016 through March 2017 for about $120 for the stem.

 

Importer: Riser Holdings Ltd., of Canada, dba Chromag Bikes

 

Manufactured in: Taiwan and Canada

********************************************************

The U.S. Consumer Product Safety Commission (CPSC) is still interested in receiving incident or injury reports that are either directly related to a product recall or involve a different hazard with the same product. Please tell us about your experience with the product on SaferProducts.gov.

 

Media Contact

Please use the phone numbers below for all media requests.

Phone: (301) 504-7908

Spanish: (301) 504-7800

 

CPSC Consumer Information Hotline

Contact us at this toll-free number if you have questions about a recall:

800-638-2772 (TTY 301-595-7054)

Times: 8 a.m. � 5:30 p.m. ET; Messages can be left anytime

Call to get product safety and other agency information and to report unsafe products.

-----------------------------

You are currently subscribed to the e-mail list "recalls" as: filter@clubhouseb.com

To unsubscribe, please do one of the following:
(1) go to https://www.cpsc.gov/en/Newsroom/Subscribe/ and use the on-line form or
(2) send a blank email to leave-3082332-722517.ab849b11e0910fe06f56217347f10a65@list.cpsc.gov

You can also go to https://www.cpsc.gov/en/Newsroom/Subscribe/ to change your
subscription, or unsubscribe an old address and subscribe a new one.

This message is from the U.S. Consumer Product Safety Commission (https://www.cpsc.gov),
an independent federal regulatory agency, located at 4330 East West
Highway, Bethesda, MD 20814  Toll-free hotline: (800) 638-2772.

 

McCain Foods USA, Inc. Expands Voluntary Recall of Frozen Hash Browns to include Wegman’s Retail Brand Due to Possible Health Risk

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

McCain Foods USA, Inc. Expands Voluntary Recall of Frozen Hash Browns to include Wegman's Retail Brand Due to Possible Health Risk

04/26/2017 05:02 PM EDT

McCain Foods USA, Inc. announced today it is expanding the voluntary recall of retail, frozen hash brown products that may contain golf ball materials, specifically hard plastic or rubber pieces, that despite our stringent supply standards may have been inadvertently harvested with potatoes used to make this product. Consumption of these products may pose a choking hazard or other physical injury to the mouth. There have been no reported injuries associated with the consumption of this product.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Our Local Bounty Recalls Organic Basil Pesto With Watercress Because of Possible Health Risk

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Our Local Bounty Recalls Organic Basil Pesto With Watercress Because of Possible Health Risk

04/26/2017 05:32 PM EDT

Our Local Bounty of Rogue River, Oregon is recalling 312 (8.5oz) containers of the Farming Fish brand Organic Basil Pesto with Watercress, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

News from CPSC: Horizon Hobby Recalls Remote-Controlled Model Vehicles Due to Fire Hazard Announced Today

 

-----------NEWS from CPSC-----------
U.S. Consumer Product Safety Commission
Office of Communications
4330 East West Highway, Bethesda, MD 20814
www.cpsc.gov

1. Horizon Hobby Recalls Remote-Controlled Model Vehicles Due to Fire Hazard: https://www.cpsc.gov/Recalls/2017/horizon-hobby-recalls-remote-controlled-model-vehicles

**********************************************************************************

1. Recall Date: April 25, 2017

Recall Number: 17-139                                                                                  

Horizon Hobby Recalls Remote-Controlled Model Vehicles Due to Fire Hazard

 

Recall Summary

 

Name of Product: ECX Circuit, Ruckus, and Torment remote-controlled model vehicles

 

Hazard: The vehicle’s electronic speed control (ESC) can fail and short circuit, posing a fire hazard.

 

Remedy: Replace

Consumers should immediately stop using the recalled product and contact Horizon Hobby for instructions on receiving a free replacement ESC.

 

Consumer Contact: Horizon Hobby at 800-338-4639 from 8 a.m. to 7 p.m. CT Monday through Friday, 8 a.m. to 5 P.M. CT on Saturday, and 12 p.m. to 5 p.m. CT on Sunday or online at www.horizonhobby.com and click on Product Recalls at the bottom of the page for more information.

 

Photos available here https://www.cpsc.gov/Recalls/2017/horizon-hobby-recalls-remote-controlled-model-vehicles

 

Recall Details

 

Units: About 18,600 (In addition, 540 were sold in Canada)

 

Description:

The recall involves the Dynamite 40-Amp FWD REV Brushed ESC – DYNS2201. It is the Electronic Speed Control (ESC) that comes in the remote controlled hobby model vehicles ECX 1/10 LiPo Circuit, Ruckus and Torment models with the following models numbers: ECX03130T1, ECX03130T2, ECX03131T1, ECX03131T2, ECX03133T1, ECX03133T2, ECX03154.  The model numbers can be found on the product box or in the owner’s manual for each vehicle. The model vehicles measure about 18 inches in length and 12 inches in width and are hobby grade remote control models for ages 14 and up.

 

Incidents/Injuries: Horizon Hobby has received 19 reports of the ESC in the model truck and cars catching fire. No injuries or property damage has been reported.

 

Sold at:  Horizon Hobby stores nationwide and online at www.horizonhobby.com from October 2016 through December 2016 for about $180.

 

Importer: Horizon Hobby LLC, of Champaign, Ill.

 

Manufactured in: China

********************************************************

The U.S. Consumer Product Safety Commission (CPSC) is still interested in receiving incident or injury reports that are either directly related to a product recall or involve a different hazard with the same product. Please tell us about your experience with the product on SaferProducts.gov.

 

Media Contact

Please use the phone numbers below for all media requests.

Phone: (301) 504-7908

Spanish: (301) 504-7800

 

CPSC Consumer Information Hotline

Contact us at this toll-free number if you have questions about a recall:

800-638-2772 (TTY 301-595-7054)

Times: 8 a.m. � 5:30 p.m. ET; Messages can be left anytime

Call to get product safety and other agency information and to report unsafe products.

-----------------------------

You are currently subscribed to the e-mail list "recalls" as: filter@clubhouseb.com

To unsubscribe, please do one of the following:
(1) go to https://www.cpsc.gov/en/Newsroom/Subscribe/ and use the on-line form or
(2) send a blank email to leave-3082046-722517.ab849b11e0910fe06f56217347f10a65@list.cpsc.gov

You can also go to https://www.cpsc.gov/en/Newsroom/Subscribe/ to change your
subscription, or unsubscribe an old address and subscribe a new one.

This message is from the U.S. Consumer Product Safety Commission (https://www.cpsc.gov),
an independent federal regulatory agency, located at 4330 East West
Highway, Bethesda, MD 20814  Toll-free hotline: (800) 638-2772.

 

Organic Herbal Supply Issues Voluntary Nationwide Recall Of All Lots Of Various Supplements For Male And Female Sexual Enhancement Due To Undeclared Active Ingredients

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Organic Herbal Supply Issues Voluntary Nationwide Recall Of All Lots Of Various Supplements For Male And Female Sexual Enhancement Due To Undeclared Active Ingredients

04/18/2017 08:25 PM EDT

Organic Herbal Supply, Inc. announced today that it is conducting a voluntary nationwide recall of all lots of Uproar, Cummor, Zrect, Monkey Business, Xrect, Rectalis, Tornado, Zdaily, BigNHard, Enhancerol Natural Male Enhancement capsules. FDA analysis has found the products to contain Tadalafil. Tadalafil is a FDA-approved drug used as treatment for male Erectile Dysfunction (ED), the presence of tadalafil in these male enhancement products renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall. Organic Herbal Supply is also recalling Zrect for Women and LabidaMAX. FDA analysis has found these two products contain Flibanserin, an FDA-approved prescription drug for Hypoactive Sexual Desire Disorder (HSDD) in women. There have been no reports of illness to date.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Party Animal Recalls Dog Food Due To Potential Presence of Pentobarbital

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Party Animal Recalls Dog Food Due To Potential Presence of Pentobarbital

04/24/2017 08:01 PM EDT

On April 13, a retailer in Texas notified us that their customer had presented samples of our 13-ounce-can Cocolicious Beef & Turkey dog food (Lot #0136E15204 04, best by July 2019) and 13-ounce-can Cocolicious Chicken & Beef dog food (Lot #0134E15 237 13, best by August 2019) to a testing lab, and that the results had tested positive for pentobarbital.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

2017-04-24 21:38:25 UPDATED: (M7.1) OFFSHORE VALPARAISO, CHILE -33.1 -72.0 (442af)

M7.1 - OFFSHORE VALPARAISO, CHILE

Preliminary Earthquake Report

Magnitude	7.1
Date-Time	24 Apr 2017 21:38:25 UTC 24 Apr 2017 17:38:25 near epicenter 24 Apr 2017 11:38:25 standard time in your timezone
Location	33.056S 72.042W
Depth	10 km
Distances	35 km (22 miles) W (275 degrees) of Valparaiso, Chile 137 km (85 miles) WNW (291 degrees) of SANTIAGO, Chile 270 km (168 miles) N (353 degrees) of Talca, Chile
Location Uncertainty	Horizontal: 4.2 km; Vertical 1.9 km
Parameters	Nph = 68; Dmin = 37.9 km; Rmss = 0.93 seconds; Gp = 81° Version =
Event ID	us 10008kce

For updates, maps, and technical information
see: Event Page or USGS Earthquake Hazards Program
National Earthquake Information Center
U.S. Geological Survey


Disclaimer

This email was sent to filter@clubhouseb.com

You requested mail for events between -90.0/90.0 latitude and 180.0/-180.0 longitude (Default World)
for M6.0 between 09:00 and 21:00 and M6.5 other times.

To change your parameters, go to: https://earthquake.usgs.gov/ens
To unsubscribe, send a one-line reply to this message with: STOP filter@clubhouseb.com

McCain Foods USA, Inc. Recalls Frozen Southern Style Hash Browns Due to Possible Health Risk. Product is Sold and Distributed Under The Roundy’s and Harris Teeter Retail Brands.

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

McCain Foods USA, Inc. Recalls Frozen Southern Style Hash Browns Due to Possible Health Risk. Product is Sold and Distributed Under The Roundy's and Harris Teeter Retail Brands.

04/21/2017 09:54 PM EDT

McCain Foods USA, Inc. announced today it is voluntarily recalling retail, frozen hash brown products that may be contaminated with extraneous golf ball materials, that despite our stringent supply standards may have been inadvertently harvested with potatoes used to make this product. Consumption of these products may pose a choking hazard or other physical injury to the mouth.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Frito-Lay Recalls Jalapeño Flavored Lay’s Kettle Cooked Potato Chips and Jalapeño Flavored Miss Vickie’s Kettle Cooked Potato Chips Due to Potential Presence of Salmonella

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Frito-Lay Recalls Jalapeño Flavored Lay's Kettle Cooked Potato Chips and Jalapeño Flavored Miss Vickie's Kettle Cooked Potato Chips Due to Potential Presence of <em>Salmonella</em>

04/21/2017 09:15 PM EDT

Frito-Lay today announced it is voluntarily recalling select Jalapeño Flavored Lay's Kettle Cooked potato chips and Jalapeño Flavored Miss Vickie's Kettle Cooked potato chips due to the potential presence of Salmonella in the seasoning.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Hospira Issues a Voluntary Nationwide Recall For One Lot Of 25% Dextrose Injection, USP (Infant) Due To The Presence of Particulate Matter

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Hospira Issues a Voluntary Nationwide Recall For One Lot Of 25% Dextrose Injection, USP (Infant) Due To The Presence of Particulate Matter

04/21/2017 07:10 PM EDT

Hospira, Inc., a Pfizer company, is voluntarily recalling one lot of 25% Dextrose Injection, USP, (Infant) pre-filled syringe to the hospital/user level due to the presence of particulate matter, identified as human hair, found within an internal sample syringe.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Hummingbird Wholesale Issues Allergy Alert on Undeclared Hazelnut in Organic Cocoa-dusted Chocolate Ginger

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Hummingbird Wholesale Issues Allergy Alert on Undeclared Hazelnut in Organic Cocoa-dusted Chocolate Ginger

04/21/2017 10:11 PM EDT

Hummingbird Wholesale of Eugene, Oregon is recalling 5lbs of Organic Cocoa-Dusted Chocolate Ginger, because it may contain undeclared hazelnut. People who have an allergy or severe sensitivity to hazelnut run the risk of serious or life-threatening allergic reaction if they consume these products.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)

Soylent Issues Allergy Alert On Potential Undeclared Milk in Soylent 1.8 Powder

You are subscribed to Recalls, Market Withdrawals and Safety Alerts for U.S. Food & Drug Administration (FDA).

This information has recently been updated and is now available.

 

 

Soylent Issues Allergy Alert On Potential Undeclared Milk in Soylent 1.8 Powder

04/24/2017 08:53 AM EDT

Soylent, Los Angeles, CA is voluntarily recalling 890 boxes of Soylent 1.8 Powder, because it may contain undeclared milk. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

For detailed information pertaining to this Recalls, Market Withdrawals and Safety Alerts message, please click the link at the beginning of this bulletin.

---

Manage your FDA Subscriptions:

• Update your preferences or unsubscribe
• Questions about this service? Please visit subscriberhelp.govdelivery.com
• Other inquiries? webmail@oc.fda.gov

---

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: U.S. Food & Drug Administration (FDA) · 10903 New Hampshire Ave · Silver Spring, MD 20993 · 1-888-INFO-FDA (1-888-463-6332)