2016-08-19 07:32:22 (M7.4) SOUTH GEORGIA ISLAND REGION -55.3 -31.9 (442af)

M7.4 - SOUTH GEORGIA ISLAND REGION

Preliminary Earthquake Report

Magnitude	7.4
Date-Time	19 Aug 2016 07:32:23 UTC 19 Aug 2016 05:32:23 near epicenter 18 Aug 2016 21:32:23 standard time in your timezone
Location	55.339S 31.939W
Depth	10 km
Distances	316 km (195 mi) ESE of Grytviken, South Georgia and the South Sandwich Islands 2297 km (1424 mi) ESE of Ushuaia, Argentina 2472 km (1532 mi) ESE of Puerto Deseado, Argentina 2478 km (1536 mi) ESE of Rio Gallegos, Argentina 1754 km (1087 mi) ESE of Stanley, Falkland Islands
Location Uncertainty	Horizontal: 8.6 km; Vertical 1.8 km
Parameters	Nph = 124; Dmin = 315.4 km; Rmss = 1.10 seconds; Gp = 23° Version =
Event ID	us 10006exl

For updates, maps, and technical information, see: Event Page or USGS Earthquake Hazards Program
National Earthquake Information Center
U.S. Geological Survey
http://earthquake.usgs.gov/regional/neic/


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

Bakers of Paris Recalls Croissants Sold at Whole Foods Market Stores in Northern California 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.

 

 

Bakers of Paris Recalls Croissants Sold at Whole Foods Market® Stores in Northern California Due to Undeclared Allergen

08/17/2016 03:53 PM EDT

Bakers of Paris (Brisbane California), is recalling plain and chocolate croissants sold in 18 Northern California Whole Foods Market stores due to an undeclared allergen. The croissants, sold individually in self-service cases and in clear plastic packs of four, are made with an egg wash which is not declared on the ingredient list.

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)

Voluntary Nationwide Recall of Cetylev® (Acetylcysteine) Effervescent Tablets for Oral Solution Due to an Inadequate Seal of the Blister Pack

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.

 

 

Voluntary Nationwide Recall of Cetylev® (Acetylcysteine) Effervescent Tablets for Oral Solution Due to an Inadequate Seal of the Blister Pack

08/18/2016 12:58 PM EDT

Arbor Pharmaceuticals, LLC (Arbor) today announced a voluntary recall of three (3) lots of Cetylev (acetylcysteine) effervescent tablets for oral solution, 500 mg, due to an inadequate seal of the blister pack. An inadequate seal could result in an increase of oxygen and moisture entering the blister cavity which can start the effervescent process. This results in enlarged and swelled tablets which could also completely dissolve within the blister pack.

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: 1 Recall 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. Xenith Recalls Football Helmets Due to Head Injury Hazard

http://www.cpsc.gov/en/Recalls/2016/Xenith-Recalls-Football-Helmets/

 

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

 

1. Xenith Recalls Football Helmets Due to Head Injury Hazard

http://www.cpsc.gov/en/Recalls/2016/Xenith-Recalls-Football-Helmets/

 

Recall Date: August 17, 2016

Recall Number: 16-245  

 

Xenith Recalls Football Helmets Due to Head Injury Hazard

http://www.cpsc.gov/en/Recalls/2016/Xenith-Recalls-Football-Helmets/  

 

Recall Summary

 

Name of Product: Football helmets

 

Hazard: The shells of the football helmets can crack, posing a risk of head injuries to football players.

 

Remedy: Replace

Football players should immediately stop using the recalled helmets.  Players, coaches and parents should contact Xenith to receive a free new replacement helmet.

Consumer Contact: Xenith at 800-956-9022 from 9 a.m. to 6 p.m. ET Monday through Friday or online at www.xenith.com and click on the “Helmet Shell Recall” link on the homepage for more information.

 

Recall Details

 

Photos Available at: http://www.cpsc.gov/en/Recalls/2016/Xenith-Recalls-Football-Helmets/

 

Units: About 5,900

 

Description: This recall involves Xenith Epic Varsity, X2 Varsity, X2E Varsity and Youth football helmets with a gloss or metallic-painted polycarbonate shell sold or factory-reconditioned between May 1, 2015 and March 18, 2016. The helmets were sold in multiple sizes depending on the model, and in varying colors and custom-paint designs. They have a facemask and a chin cup, available in different styles and varying colors, and may have an optional eye shield. The serial number is printed on a white sticker inside the top of the helmet. A complete list of the serial numbers included in this recall is available at www.xenith.com/recall.

 

Incidents/Injuries: The firm received 29 reports of cracking helmets; no injuries reported.

 

Sold at: Through team dealers and direct school sales, and at BSN, Buddy’s All Stars, Carey’s Sporting Goods, End Zone Sports and Sports, Inc. and other stores nationwide and online at Eastbay.com, Footlocker.com, SafetyFirstSports.com, SportsUnlimitedInc.com and Xenith.com from May 2015 through March 2016 for between $140 and $400.

 

Manufacturer: Xenith LLC, of Detroit, Mich.

 

Manufactured in: U.S.

 

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

 

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

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/cpsclist.aspx and use the on-line form or
(2) send a blank email to leave-3053841-722517.ab849b11e0910fe06f56217347f10a65@list.cpsc.gov

You can also go to http://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 (www.cpsc.gov),
an independent federal regulatory agency, located at 4330 East West
Highway, Bethesda, MD 20814  Toll-free hotline: (800) 638-2772.

 

Sage Products Expands Voluntary Nationwide Recall of Comfort Shield Barrier Cream Cloths Due to Microbial Contamination

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.

 

 

Sage Products Expands Voluntary Nationwide Recall of Comfort Shield Barrier Cream Cloths Due to Microbial Contamination

08/17/2016 11:19 AM EDT

Cary, IL, Sage Products announced today it is expanding its voluntary nationwide recall to include an additional lot of Comfort Shield Barrier Cream Cloths at the distributor and healthcare facility/user level. The recall is being initiated due to product contamination with the bacteria, Burkholderia cepacia.

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)

Cook Medical Issues Global Recall of Roadrunner® UniGlide® Hydrophilic Wire Guides due to raw materials issue

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.

 

 

Cook Medical Issues Global Recall of Roadrunner® UniGlide® Hydrophilic Wire Guides due to raw materials issue

08/15/2016 03:16 PM EDT

DSM Biomedical B.V., the Netherlands, Cook Medical's supplier of hydrophilic coating for the Roadrunner® Uniglide® Hydrophilic Wire Guide, recalled certain lots of material due to concerns about a potential contamination by glass particles ranging in size of approximately 4 to 280 µm. Cook received one lot of the affected recalled coating. This prompted Cook Medical to initiate a recall of 8,750 units of the Roadrunner UniGlide Hydrophilic Wire Guides on June 24, 2016.

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)

Oriental Packing Co., Inc. Issues Alert on Lead in Curry 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.

 

 

Oriental Packing Co., Inc. Issues Alert on Lead in Curry Powder

08/12/2016 05:25 PM EDT

Oriental Packing Co., Inc., Miami, Florida is recalling approximately 377,000 lbs. of the following blended seasoning curry products because it is contaminated with lead. Lead can accumulate in the body over time and can cause serious and sometimes permanent adverse health consequences

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)