Friday, February 10, 2017

PetSmart Voluntarily Recalls Single Lot of Grreat Choice® Canned Dog Food 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.

 

 

02/10/2017 02:56 PM EST

PetSmart has issued a voluntary recall of one production lot of its Grreat Choice® Adult Dog Food sold on PetSmart.com, Pet360.com, PetFoodDirect.com and in nationwide PetSmart retail stores. This product is being voluntarily recalled as a precautionary measure due to metal contamination that could potentially be a choking hazard to pets.

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


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) Powered by GovDelivery

News from CPSC: La-Z-Boy Recalls Power Supplies Sold With Lift Chairs Due to Shock Hazard Announced February 8, 2017

 

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

1. La-Z-Boy Recalls Power Supplies Sold With Lift Chairs Due to Shock Hazard: https://www.cpsc.gov/Recalls/2017/La-Z-Boy-Recalls-Power-Supplies-Sold-With-Lift-Chairs

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

1. Recall Date: February 8, 2017

Recall Number: 17-083

La-Z-Boy Recalls Power Supplies Sold With Lift Chairs Due to Shock Hazard

 

Recall Summary

 

Name of Product: Power supplies sold with lift chairs

 

Hazard: The lift chair’s power supply cover can crack within the screw housing and break, causing the cover to detach and exposing the power supply’s electrical components, posing a shock hazard to users.

 

Remedy:  Replace

                                                        

Consumers should immediately stop using the power supplies to power the lift chairs and contact La-Z-Boy for a free replacement power supply.

 

Consumer Contact:  La-Z-Boy toll-free at 855-592-9087 from 9 a.m. to 5 p.m. ET Monday through Friday or online at www.la-z-boy.com and click on the Recall button for more information. 

 

Photos available at: https://www.cpsc.gov/Recalls/2017/La-Z-Boy-Recalls-Power-Supplies-Sold-With-Lift-Chairs

 

Recall Details

 

Units:  About 2,500 (In addition, 210 were sold in Canada)

 

Description: The recall involves the power supplies sold with Gold Series electric Lift Chairs, the Clayton Luxury-Lift (Model 1HL562) and Power Lift (Model 1ML562), and Luxury-Lift (Models 1LF505 and 1LF819). They were also part of conversion kits for older lift chairs with Models 1LL320, 1LL508, 1LL515, 1LM320, 1LM508 and 1LM515. The power supply enables the chair’s seat to lift a consumer from a seated into a standing position. The power supply casing is a black, plastic rectangular box measuring approximately 6 inches by 3½ inches by 3½ inches.  Only power supplies with LOT #150113 are included in this recall.  The model name, model number and lot number are printed on the back of the power supply.

 

Incidents/Injuries: None reported

 

Sold at: La-Z-Boy Furniture Galleries and independent furniture stores nationwide and online at la-z-boy.com from September 2015 through November 2016 for between $1,900 and $2,800. The power supplies were also sold separately for about $170 and provided free under warranty as replacements for use with previously-purchased chairs. 

 

Distributor: La-Z-Boy Incorporated, of Monroe, Mich.

 

Importer: LogicData North America, of Grand Rapid, Mich. (power supply)

 

Manufactured in: China (power supplies), U.S. (lift chairs)

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

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-3072200-722517.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.

 

2017-02-10 14:03:45 UPDATED: (M6.5) MINDANAO, PHILIPPINES 9.9 125.5 (442af)

M6.5 - MINDANAO, PHILIPPINES

Preliminary Earthquake Report
Magnitude 6.5
Date-Time
  • 10 Feb 2017 14:03:46 UTC
  • 10 Feb 2017 22:03:46 near epicenter
  • 10 Feb 2017 04:03:46 standard time in your timezone
Location 9.899N 125.463E
Depth 27 km
Distances
  • 10 km (6 mi) NNE of Mabua, Philippines
  • 12 km (7 mi) NNW of Surigao, Philippines
  • 31 km (19 mi) NNW of Placer, Philippines
  • 72 km (44 mi) ESE of Maasin, Philippines
  • 713 km (442 mi) SE of Manila, Philippines
Location Uncertainty Horizontal: 5.8 km; Vertical 4.8 km
Parameters Nph = 233; Dmin = 312.8 km; Rmss = 0.84 seconds; Gp = 52°
Version =
Event ID us 20008ixa

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 'AT00ol5web' exclusion region, but was large enough to trigger notification.
To change your parameters, go to: https://sslearthquake.usgs.gov/ens
To unsubscribe, send a one-line reply to this message with: STOP filter@clubhouseb.com

Thursday, February 9, 2017

Legendary Baking Issues Allergy Alert-Almonds and Egg in Salted Caramel Chocolate Almond Pie Allergens Declared but Listed Under “May Contain”

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.

 

 

02/09/2017 11:02 AM EST

Legendary Baking of Denver, CO, is recalling its 34 ounce packages of Private Selection Salted Caramel Chocolate Almond Pie because the almonds and eggs were listed under "may contains" instead of "contains". People who have allergies to almonds and eggs 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.


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) Powered by GovDelivery

Exela Pharma Sciences, LLC Issues Voluntary Nationwide Recall of Ibuprofen Lysine Injection, 20 Mg/2 Ml (10 Mg/Ml) Due to 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.

 

 

02/08/2017 07:33 PM EST

Exela Pharma Sciences, LLC ("Exela"), in association with marketer X-Gen Pharmaceuticals, Inc. ("X-Gen"), is voluntarily recalling lot number PLND1613 of Ibuprofen Lysine Injection, 20 mg /2 mL (10 mg/mL), vials to the hospital or user level. Some of the vials have been found to contain particulate matter.

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


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) Powered by GovDelivery

Ruth’s Salad Charlotte NC Expands Recall of Ruth’s Salads Pimento Spreads due to Possible Health Risk. May Contain Listeria Monocytogenes

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.

 

 

02/09/2017 12:32 PM EST

Ruth's Salads Charlotte, NC is expanding the recall of Ruth's Salads Pimento Cheese Spreads packed in Chester, SC. The products involved include: Ruth's Original Pimento Spread 7oz; Ruth's Original Pimento Spread 12 oz.; Ruth's Original Pimento Spread 24 oz.; Ruth's Old Fashion Pimento Spread 16 oz.; Ruth's Jalapeno Pimento Spread 12 oz.; Ruth's Lite Pimento Spread 12 oz.; and Ruth's Cream Cheese with Pineapple-Pecans 12 oz.

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


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) Powered by GovDelivery

Wednesday, February 8, 2017

Kingsway Trading Inc. Recalls “Xanthium & Siler Combo (Bi Yan Pian) Dietary Supplement” because it Contains Banned Ephedra Alkaloids

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.

 

 

02/08/2017 10:20 AM EST

Kingsway Trading Inc. of Brooklyn, NY is recalling its 1.06 oz (30g) bottles of "Well Balance Xanthium & Siler Combo (Bi Yan Pian)" Batch No. 130401 & Batch No. 150201 because they contain the presence of undeclared Ephedra Herba (ma huang), an FDA banned item. Dietary supplements containing ephedrine alkaloids pose a risk of serious adverse events, including heart attack, stroke, and death, and that these risks are unreasonable in light of any benefits that may result from the use of these products under their labeled conditions of use, or under ordinary conditions of use if the labeling is silent.

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


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) Powered by GovDelivery

Fred Meyer Stores Issues Allergy Alert on Fred Meyer 100% Whole Wheat Bread due to Undeclared Milk

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.

 

 

02/08/2017 11:27 AM EST

Fred Meyer Stores has recalled the 16 oz Fred Meyer 100% Whole Wheat Bread sold in its retail stores because the product may contain nonfat dry milk not listed on the label. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume 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.


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) Powered by GovDelivery

Too Loud! For Too Long!: CDC Vitalsigns Report

About 40 million Americans aged 12 years and older have hearing loss.
Having trouble viewing this email? View it as a Web page.
Download Factsheet
Vitalsigns

CDC

 
Too Loud! For Too Long!

Too Loud!
For Too Long!

Loud noises damage hearing

 
 

February 8, 2017

 

Ask. Test. Counsel.

Hearing loss


[PDF, 1.9 MB, 4 Pages]

Hearing loss is the third most common chronic health condition in the US. Almost twice as many people report hearing loss as report diabetes or cancer. Noise exposure away from your job can damage your hearing just as much as working in a noisy place. Being around too much loud noise—like using a leaf blower or going to loud concerts—can cause permanent hearing loss. And once it's gone, you can't get it back! You can have hearing loss before you even notice you're having problems.

Key points include:

  • About 40 million US adults aged 20-69 years have noise-induced hearing loss.

  • More than 1 in 2 US adults with hearing damage from noise do not have noisy jobs.

  • About 1 in 4 US adults who report excellent to good hearing already have hearing damage.

 
About 40 million US adults aged 20-69 years have noise-induced hearing loss. Learn more.
 
Vital Signs is a monthly report that appears as part of the CDC journal, Morbidity and Mortality Weekly Report.
Content source: Office of the Associate Director for Communications (OADC)
Dept of Health and Human Services Logo  CDC 24/7 - Saving Lives, Protecting People, Saving Money. CDC.gov/24-7
CDC on Facebook   CDC on Twitter   CDC YouTube Channel  CDC Instagram   CDC Pinterest
CDC Vital Signsô ñ Learn about the latest public health data. Read CDC Vital SignsôÖ

This email was sent to filter@clubhouseb.com using GovDelivery, on behalf of: Centers for Disease Control and Prevention • 1600 Clifton Rd • Atlanta, GA 30333 • 1-800-CDC-INFO (800-232-4636) Powered by GovDelivery

Starway Inc. Issues an Alert on Undeclared Sulfites in Peony Mark Brand Dried Lily Flower

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.

 

 

02/07/2017 05:42 PM EST

Starway Incorporated, located at 137 Grattan Street, Brooklyn, NY, 11237, is recalling Peony Mark Brand Dried Lily Flower because the product contains undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life threatening allergic reactions if they consumer 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.


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) Powered by GovDelivery

Tuesday, February 7, 2017

2017-02-07 22:03:54 (M6.3) SOUTHWESTERN PAKISTAN 25.2 63.2 (442af)

M6.3 - SOUTHWESTERN PAKISTAN

Preliminary Earthquake Report
Magnitude 6.3
Date-Time
  • 7 Feb 2017 22:03:54 UTC
  • 8 Feb 2017 03:03:54 near epicenter
  • 7 Feb 2017 12:03:54 standard time in your timezone
Location 25.208N 63.245E
Depth 10 km
Distances
  • 23 km (14 mi) WSW of Pasni, Pakistan
  • 90 km (55 mi) SSE of Turbat, Pakistan
  • 93 km (57 mi) E of Gwadar, Pakistan
  • 140 km (86 mi) W of Ormara, Pakistan
  • 503 km (311 mi) ENE of Muscat, Oman
Location Uncertainty Horizontal: 8.6 km; Vertical 1.8 km
Parameters Nph = 120; Dmin = 710.5 km; Rmss = 0.89 seconds; Gp = 28°
Version =
Event ID us 20008ic7

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://sslearthquake.usgs.gov/ens
To unsubscribe, send a one-line reply to this message with: STOP filter@clubhouseb.com