2017-06-17 22:26:02 (M6.1) SOUTH OF FIJI ISLANDS -24.1 179.6 (442af)

M6.1 - SOUTH OF FIJI ISLANDS

Preliminary Earthquake Report

Magnitude	6.1
Date-Time	17 Jun 2017 22:26:03 UTC 18 Jun 2017 10:26:03 near epicenter 17 Jun 2017 12:26:03 standard time in your timezone
Location	24.105S 179.591E
Depth	518 km
Distances	675 km (420 miles) S (170 degrees) of SUVA, Fiji 1492 km (927 miles) NNE (19 degrees) of Auckland, New Zealand
Location Uncertainty	Horizontal: 7.7 km; Vertical 6.0 km
Parameters	Nph = 149; Dmin = 620.4 km; Rmss = 0.88 seconds; Gp = 34° Version =
Event ID	us 20009nc2

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


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Willis Ocean Inc Issues Alert on Uneviscerated Scomber Fish

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Willis Ocean Inc Issues Alert on Uneviscerated Scomber Fish

06/16/2017 09:43 AM EDT

Willis Ocean Inc., Brooklyn, NY, is recalling its "the duck" brand "frozen steamed scomber fish", because the product was found to be uneviscerated. The steamed scomber fish were distributed nationwide through retail stores.

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NOW Health Group Inc. Expands Voluntary Recall of Ellyndale® Nutty Infusions™ Because of Possible Health Risk

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NOW Health Group Inc. Expands Voluntary Recall of Ellyndale® Nutty Infusions™ Because of Possible Health Risk

06/16/2017 09:15 AM EDT

NOW Health Group, Inc. (NOW), of Bloomingdale, Illinois, is expanding the voluntary recall of Ellyndale® Nutty Infusions™ Roasted Cashew Butter – Product Code E0540, Lot# 2125155, and Ginger Wasabi Cashew Butter -- Product Code E0541, Lot# 2124118, to include Roasted Almond Butter – Product Code E0545, Lot# 2124119, and Mango Chili Cashew Butter – Product Code E0542, Lot# 2125156. An FDA follow-up inspection of the Nutty Infusions supplier's facility revealed these lots have 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.

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Hospira Issues a Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection, USP, Neut tm (Sodium Bicarbonate 4% Additive Solution), QUELICIN tm (Succinylcholine Chloride Injection, USP) and Potassium Phosphates Injection, USP Due To a Potential For Lack Of Sterility Assurance

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Hospira Issues a Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection, USP, Neut ^tm (Sodium Bicarbonate 4% Additive Solution), QUELICIN ^tm (Succinylcholine Chloride Injection, USP) and Potassium Phosphates Injection, USP Due To a Potential For Lack Of Sterility Assurance

06/16/2017 07:26 AM EDT

Hospira, Inc., a Pfizer company, is voluntarily recalling 42 lots of 8.4% Sodium Bicarbonate Injection, USP, 50 mL vials, 5 lots of NeutTM (Sodium Bicarbonate 4% additive solution) 5 mL vials, 5 lots of QUELICINTM (Succinylcholine Chloride Injection, USP) 200 mg/10 mL vials and 7 lots of Potassium Phosphates Injection, USP, 45 mM vials to the hospital/retail level due to microbial growth detected during a routine simulation of the manufacturing process, which represents the potential introduction of microorganisms into the products.

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Teva Pharmaceuticals, USA Extends Voluntary Nationwide Recall to Consumer/User Level for One Lot of Paliperidone Extended-Release Tablets, 3mg, 90 Count Bottles Distributed Under the Actavis Pharma Inc. Label Due to Dissolution Test Failure

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Teva Pharmaceuticals, USA Extends Voluntary Nationwide Recall to Consumer/User Level for One Lot of Paliperidone Extended-Release Tablets, 3mg, 90 Count Bottles Distributed Under the Actavis Pharma Inc. Label Due to Dissolution Test Failure

06/15/2017 02:09 PM EDT

Teva Pharmaceuticals USA, Inc. (Teva) initiated a voluntary recall to retail-level on 05/31/2017 for one lot of Paliperidone Extended-Release Tablets, 3mg, 90 count bottles that was distributed under the Actavis Pharma Inc. label. In coordination with FDA, Teva is extending this recall to the CONSUMER/USER level.

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Advanced Pharma, Inc. D/B/A Avella of Houston Issues Voluntary Nationwide Recall of All Unexpired Nitroglycerin Injection In 5% Dextrose USP Products Produced At Its Houston Location From March 3, 2017 Through May 31, 2017 Due To Sub-Potency

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Advanced Pharma, Inc. D/B/A Avella of Houston Issues Voluntary Nationwide Recall of All Unexpired Nitroglycerin Injection In 5% Dextrose USP Products Produced At Its Houston Location From March 3, 2017 Through May 31, 2017 Due To Sub-Potency

06/15/2017 05:53 PM EDT

Advanced Pharma, Inc. d/b/a Avella of Houston ("Advanced Pharma") is voluntarily recalling all unexpired lots of Nitroglycerin products that were produced at Advanced Pharma's Houston location between March 3, 2017 and May 31, 2017 to the hospital/user level. The recall is being issued based on laboratory test results indicating a lower than expected potency on certain lots of compounded NitroGlycerin Injection which would lead to a lower dose being administered.

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New England Natural Bakers Issues Voluntary Recall Due to Possible Health Risk

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New England Natural Bakers Issues Voluntary Recall Due to Possible Health Risk

06/15/2017 05:43 PM EDT

NEW ENGLAND NATURAL BAKERS of Greenfield MA, is issuing a voluntary recall, the company has been notified by an ingredient supplier that an ingredient used in these products has the potential to be contaminated with Listeria monocytogenes.

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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. Little Giraffe Recalls Children’s Robes Due to Violation of Federal Flammability Standard:  https://www.cpsc.gov/Recalls/2017/Little-Giraffe-Recalls-Childrens-Robes
 

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

1. Recall Date: June 15, 2017

Recall Number: 17-178               

Little Giraffe Recalls Children’s Robes Due to Violation of Federal Flammability Standard
 

Recall Summary

 

Name of Product: Luxe Satin children’s robes

 

Hazard: The children’s robes fail to meet the federal flammability standards for children’s sleepwear, posing a risk of burn injuries to children.

 

Remedy: Refund

Consumers should immediately take the recalled robes away from children and contact Little Giraffe for a full refund.  
 

Consumer Contact: Little Giraffe toll-free at (866) 201-6613 from 10 a.m. to 4 p.m. PT Monday through Friday or online at www.littlegiraffe.com and click on “Recall Information” at the bottom of the page for more information.

 

Pictures available here:  https://www.cpsc.gov/Recalls/2017/Little-Giraffe-Recalls-Childrens-Robes

 

 

Recall Details

 

Units: About 2,000

 

Description: 

This recall involves Luxe Satin children’s long-sleeve robes. The robes are 43 percent acetate with 57 percent rayon, satin outer shell and a 100 percent polyester microfiber inside. The robes were sold in pink, blue and cream in sizes 1 (XS-S/4-6 years), 2 (MD-LG/6-8 years) and 3 (XL-XXL/8-10 years). The robes have two belt loops on each side and an unattached belt. Lot number “21706-DFR001” and “Not Intended for Sleepwear” are printed on the robes inside seam label.   
 

Incidents/Injuries: 
None reported

 

Sold at: Children’s specialty stores nationwide and online at www.littlegiraffe.com from November 2012 through March 2017 for about $100.  

 

Importer(s):

Little Giraffe, of Van Nuys, Calif.

 

Distributor(s):

Little Giraffe, of Van Nuys, Calif.

 

Manufactured In:

China

 

*****!!! Unless otherwise stated, any views or opinions expressed in this e-mail (and any attachments) are solely those of the author and do not necessarily represent those of the U.S. Consumer Product Safety Commission. Copies of product recall and product safety information can be sent to you automatically via Internet e-mail, as they are released by CPSC. To subscribe or unsubscribe to this service go to the following web page: http://www.cpsc.gov/en/Newsroom/Subscribe *****!!!   

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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

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Phone: (301) 504-7908

Spanish: (301) 504-7800

 

CPSC Consumer Information Hotline

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Bulletproof 360, Inc. Recalls Collagen Protein Bars and Bites Because of Possible Health Risk

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Bulletproof 360, Inc. Recalls Collagen Protein Bars and Bites Because of Possible Health Risk

06/15/2017 07:00 AM EDT

– Bulletproof 360, Inc. ("Bulletproof") of Bellevue, Washington is recalling five Collagen Protein Bar and Bite products because they have 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.

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Gomacro Recalls Limited Number of Macrobars and Thrive Bars Because of Possible Health Risk

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Gomacro Recalls Limited Number of Macrobars and Thrive Bars Because of Possible Health Risk

06/15/2017 09:53 AM EDT

GoMacro, of Viola, Wis., is recalling a limited number of MacroBars and Thrive Bars because they have 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.

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Kroger Expands Recall of 12 oz. packages of Simple Truth Dry Roasted Macadamia Nuts because of Possible Health Risk

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Kroger Expands Recall of 12 oz. packages of Simple Truth Dry Roasted Macadamia Nuts because of Possible Health Risk

06/15/2017 11:55 AM EDT

The Kroger Co. (NYSE: KR) today announced it has expanded the recall of its 12 oz. packages of Simple Truth Dry Roasted Macadamia Nuts due to potential Listeria monocytogenes contamination. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

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Wildway LLC Issues Voluntary Recall of Certain Grain-Free Granola Products

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Wildway LLC Issues Voluntary Recall of Certain Grain-Free Granola Products

06/14/2017 09:29 PM EDT

Wildway LLC is voluntarily recalling certain grain-free granola codes, because the Company has been notified by an ingredient supplier that an ingredient used in these products has the potential to be contaminated with Listeria monocytogenes.

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Loving Pets Voluntarily Recalls Limited Lot Numbers of Air-Puffed Dog Treats Because of Possible Salmonella Health Risk

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Loving Pets Voluntarily Recalls Limited Lot Numbers of Air-Puffed Dog Treats Because of Possible Salmonella Health Risk

06/14/2017 05:26 PM EDT

Loving Pets of Cranbury, NJ is voluntarily recalling a limited number of dog treats because of the potential to be contaminated with Salmonella. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products.

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Phillips Company Issues Voluntary Worldwide Recall of All Topical Products Due to Concerns of Manufacturing Practices

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Phillips Company Issues Voluntary Worldwide Recall of All Topical Products Due to Concerns of Manufacturing Practices

06/14/2017 02:42 PM EDT

Phillips Company is voluntarily recalling all lots of Tetrastem, Diabecline, Tetracycline-ABC, VenomX, Acneen, StaphWash, StringMed, NoPain and LidoMed distributed by Phillips Company, with business offices located in Sun City, Arizona, to the retail level. The products are being recalled after an FDA inspection found significant manufacturing practices that calls into question the safety, identity, strength, quality and purity of unexpired drug products made at the firm during the past three years.

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2017-06-14 07:29:06 UPDATED: (M6.9) GUATEMALA 15.0 -91.9 (442af)

M6.9 - GUATEMALA

Preliminary Earthquake Report

Magnitude	6.9
Date-Time	14 Jun 2017 07:29:07 UTC 14 Jun 2017 01:29:07 near epicenter 13 Jun 2017 21:29:07 standard time in your timezone
Location	15.019N 91.928W
Depth	111 km
Distances	15 km (10 miles) WNW (296 degrees) of San Marcos, San Marcos, Guatemala 26 km (16 miles) E (80 degrees) of Cacahoat���n, Chiapas, Mexico 40 km (25 miles) ENE (71 degrees) of Tapachula, Chiapas, Mexico 158 km (98 miles) WNW (286 degrees) of GUATEMALA CITY, Guatemala
Location Uncertainty	Horizontal: 8.3 km; Vertical 3.3 km
Parameters	Nph = 83; Dmin = 56.4 km; Rmss = 1.15 seconds; Gp = 46° Version =
Event ID	us 20009mbt

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


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News from CPSC: 2 Recalls 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. GTHI Recalls Climbing Belay Devices Due to Fall and Injury Hazards: https://www.cpsc.gov/Recalls/2017/GTHI-Recalls-Climbing-Belay-Devices

2. Noble House Recalls Chairs Due to Fall Hazard: https://www.cpsc.gov/Recalls/2017/Noble-House-Recalls-Chairs
 

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

1. Recall Date: June 13, 2017

Recall Number: 17-176                  

GTHI Recalls Climbing Belay Devices Due to Fall and Injury Hazards
 

Recall Summary

 

Name of Product: Vergo belay devices (climbing tool)

 

Hazard: The handle on the Vergo belay device can loosen and cause the device’s assisted braking capacity to malfunction, posing fall and injury hazards to climbers.

 

Remedy: Replace

Consumers should immediately stop using the recalled devices and contact Trango for instructions on receiving a free replacement.

 

Consumer Contact: Trango email at vergorecall@trango.com, or call 800-860-3653 from 8 a.m. to 4 p.m. MT, Monday through Friday, or online at www.trango.com   and click on “Product Alerts” for more information.

 

Pictures available here:  https://www.cpsc.gov/Recalls/2017/GTHI-Recalls-Climbing-Belay-Devices

 

 

Recall Details

 

Units: About 2,600 (in addition, about 100 were sold in Canada)

 

Description: 

This recall involves Trango Vergo belay devices with batch numbers 16159 and 16195 printed on the side of the unit. The devices were sold in blue, gold, or purple and feature the word “VERGO” on the front plate of the unit. Belay devices are used with climbing ropes to protect the climber while climbing, to arrest a fall or while being lowered on the rope.
 

Incidents/Injuries: 
The firm has received three reports of the belay device’s handle over-rotating and braking malfunction. No injuries have been reported.

 

Sold at: Authorized GTHI dealers and outdoor specialty stores nationwide and online at www.trango.com from October 2016 through April 2017 for about $90.

 

Distributor(s):

Great Trango Holdings Inc. (GTHI), of Lafayette, Colo.

 

Manufactured In:

United States

 

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

2. Recall Date: June 13, 2017

Recall Number: 17-177                  

Noble House Recalls Chairs Due to Fall Hazard
 

Recall Summary

 

Name of Product: Dining chairs

 

Hazard: The legs of the chairs can break, posing a fall hazard to consumers.

 

Remedy: Repair

Consumers should immediately stop using the recalled chairs and contact Noble House for a free repair kit including shipping.  

 

Consumer Contact: Noble House toll-free at 888-600-6376 from 8 a.m. to 5 p.m. PT Monday through Friday or online at www.noblehousefurniture.com and click on the Safety Recall Link located under the Contact Us tab at the bottom of the page.

 

Pictures available here:  https://www.cpsc.gov/Recalls/2017/Noble-House-Recalls-Chairs

 

 

Recall Details

 

Units: About 3,300

 

Description: 

This recall involves Noble House’s Kaius, Henrietta, and Fauna dining chairs which have solid wood legs and an upholstered seat. The Kaius Fabric chairs have a curved, wood back and fabric cushion and measure 21 inches deep by 23 inches wide by 30 inches high.  The Henrietta Fabric chairs have a cushioned seat and back and measure 21 inches deep by 22 inches wide by 32 inches high.  The Fauna Dining chairs have a cushioned seat and back and measures 20 inches deep by 20 inches wide by32 inches high. The recalled chairs have a label underneath the seat that reads “MADE FOR: NOBLE HOUSE HOME FURNISHINGS LLC: 21325 Superior St., Chatsworth CA 91311.”
 

Incidents/Injuries: 
The firm has received six reports of the chairs breaking, with four incidents resulting in consumers receiving bruises from falls.

 

Sold at: Online at Amazon, Overstock and Wayfair, and from September 2016 through March 2017 for about $130.

 

Importer(s):

Noble House Home Furnishings LLC, of Chatsworth, Calif.

 

 

Distributor(s):

Noble House Home Furnishings LLC, of Chatsworth, Calif.

 

Manufactured In:

Malaysia

 

*****!!! Unless otherwise stated, any views or opinions expressed in this e-mail (and any attachments) are solely those of the author and do not necessarily represent those of the U.S. Consumer Product Safety Commission. Copies of product recall and product safety information can be sent to you automatically via Internet e-mail, as they are released by CPSC. To subscribe or unsubscribe to this service go to the following web page: http://www.cpsc.gov/en/Newsroom/Subscribe *****!!!   ­­  

 

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

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

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