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      J&J Settles Talc Mesothelioma Settlement

      By Sandra Dalton, Staff Writer On January 6, 2020, Superior Court Judge Stephen Kaus announced that Johnson & Johnsons (J&J) had agreed to … [Read More...]

      509 Recalls Helmets Due to Risk of Head Injury

      The recalled helmets fail to provide sufficient protection in the event of a crash, posing a risk of head injury. … [Read More...]

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Arctic Zero Inc. Voluntarily Recalls For Relabeling Frozen Dessert Due To Undeclared Milk Allergen On Label.

July 6, 2012 By The FDA Leave a Comment

Arctic Zero Inc. of Escondido, Ca. is voluntarily recalling to relabel pints and chocolate dipped bars which were produced before February of 2012, due to undeclared milk allergen. All products that were produced after February 2012 have the statement "Contains whey protein, which is a derivative of dairy". Whey protein is considered a derivative … [Read more...]

Filed Under: FDA Press Releases

Pacific International Marketing Voluntarily Recalls 19 Cases of Bulk Romaine Lettuce Sold At Vons And Pavilions Stores In California And NevadaDue To Possible Salmonella Contamination

July 6, 2012 By The FDA Leave a Comment

Pacific International Marketing ("Pacific") is voluntarily recalling 19 cases of bulk Romaine Lettuce sold at Vons and Pavilions stores in California and Nevada due to potential Salmonella contamination. The bulk Romaine Lettuce was sold in bulk produce bins from July 2, 2012 through July 4, 2012. The lettuce heads are banded with a red twist tie … [Read more...]

Filed Under: FDA Press Releases

Expanded Voluntary Recall of Mazuri® Feed Products Due to Potential ElevatedVitamin D Level

July 6, 2012 By The FDA Leave a Comment

PMI Nutrition International is expanding a voluntary recall to include three additional varieties of the Mazuri® feed products listed below, due to the potential for an elevated vitamin D level in these products. Elevated vitamin D levels can be harmful to animals if fed for extended periods, and may result in lack of interest in eating, weight … [Read more...]

Filed Under: FDA Press Releases

Stryker Initiates Voluntary Product Recall of Modular-Neck Stems Action Specific to Rejuvenate and ABG II Modular-Neck Stems

July 6, 2012 By The FDA Leave a Comment

Stryker has voluntarily recalled its Rejuvenate and ABG II modular-neck stems. "While modular-neck stems provide surgeons with an option to correct certain aspects of a patient's anatomy and hip biomechanics, given the potential risks associated with fretting and corrosion at the modular neck junction, Stryker Orthopaedics decided to take this … [Read more...]

Filed Under: FDA Press Releases

BEDFORD LABORATORIES™ ISSUES NATIONWIDE VOLUNTARY HOSPITAL/USER‐LEVEL RECALL OF LEUCOVORIN CALCIUM INJECTION

July 6, 2012 By The FDA Leave a Comment

  Contact: Consumer: For Information: 1-800-562-4797 Adverse Reactions: 1-800‐521‐5169 Media: Marjorie Moeling, 440-703-7525 marjorie.moeling@boehringer‐ingelheim.com   FOR IMMEDIATE RELEASE - July 3, 2012 -Bedford Laboratories™ today announced a nationwide voluntary hospital/user‐level recall for: Product Description NDC … [Read more...]

Filed Under: FDA Press Releases

BI-LO Issues Class II Recall On Southern Home Brand Bacon Ranch Salad Mix & Creamy Parmesan Salad Mix

July 6, 2012 By The FDA Leave a Comment

 Contact:Consumer:BI-LO Customer Relations1-800-862-9293Media:Amanda LenarErwin Penland864-672-2810amanda.lenar@erwinpenland.com  FOR IMMEDIATE RELEASE - June 29, 2012 - Today BI-LO announced an immediate Class II voluntary recall of two store brand products, the Southern Home® Bacon Ranch Salad Mix and the Southern Home® … [Read more...]

Filed Under: FDA Press Releases

Bath Petals Recalls Soy Candles Due to Fire and Laceration Hazard

July 6, 2012 By The CPSC Leave a Comment

p>WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission and Health Canada, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer … [Read more...]

Filed Under: CPSC Press Releases

iSi North America Recalls Twist’n Sparkle Beverage Carbonation System Due to Explosion Hazard

July 6, 2012 By The CPSC Leave a Comment

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product. Name of … [Read more...]

Filed Under: CPSC Press Releases

PREVOST ( 12V300000 )

July 5, 2012 By NHTSA Leave a Comment

Vehicle Make / Model:     Model Year(s):      PREVOST / VIP 45     2012      PREVOST / X3-45     2012      PREVOST / XLII     2012 Manufacturer: PREVOST CARS, INC. Mfr's Report Date: JUN 27, 2012 NHTSA CAMPAIGN ID Number: … [Read more...]

Filed Under: NHTSA Press Releases

CHEVROLET ( 12V301000 )

July 5, 2012 By NHTSA Leave a Comment

Vehicle Make / Model:     Model Year(s):      CHEVROLET / CAPTIVA SPORT     2012 Manufacturer: GENERAL MOTORS LLC Mfr's Report Date: JUN 26, 2012 NHTSA CAMPAIGN ID Number: 12V301000 N/A NHTSA Action Number: N/A Component: PARKING BRAKE Potential Number of Units Affected: 2,070 Summary: … [Read more...]

Filed Under: NHTSA Press Releases

***UPDATED CONSUMER ALERT*** Listeria Contamination in Certain Mexicali Cheese Corp. Products

July 4, 2012 By The FDA Leave a Comment

 Contact:Consumer:Jessica Chittenden Ziehm518-457-3136FOR IMMEDIATE RELEASE - July 2, 2012 - New York State Agriculture Commissioner Darrel Aubertine today warned consumers in the metropolitan New York area, including Queens, the Bronx, and Brooklyn, to not consume certain cheese products made by Mexicali Cheese Corp. located at 91-52 87th … [Read more...]

Filed Under: FDA Press Releases

CareFusion Provides Update On Voluntary Recall Of Select AirLifeâ„¢ Respiratory Products

July 4, 2012 By The FDA Leave a Comment

 Contact:Consumer:CareFusion Customer Service Customer.Experience@carefusion.comMedia:Kristen Cardillokristen.cardillo@carefusion.com 858-617-2317Investors:Jim Mazzola858-617-1203jim.mazzola@carefusion.com  FOR IMMEDIATE RELEASE - July 2, 2012 - CareFusion issued the following update regarding its voluntary recall of its … [Read more...]

Filed Under: FDA Press Releases

Voluntary Recall of LabDie and Mazuri Feed Products

July 4, 2012 By The FDA Leave a Comment

  Contact Consumer: 1-855-863-0421, x224 Media: Trish Scorpio, PMI International 651-375-1814 FOR IMMEDIATE RELEASE – July 3, 2012 – PMI Nutrition International has initiated a voluntary recall of four varieties of the LabDiet® and Mazuri® feed products listed below, due to the potential for an elevated vitamin D level in … [Read more...]

Filed Under: FDA Press Releases

URGENT: Recalling Due to Undeclared Eggs

July 4, 2012 By The FDA Leave a Comment

  Contact Consumer: (562) 404-2568 info@fruitipops.com Media: Fruiti Pops, Inc. Jr. Aguado (562) 404-2568 FOR IMMEDIATE RELEASE - July 3, 2012 - Fruiti Pops, Inc. is recalling 178 dozen Fruiti Pops 4 ounce Classic Coconut frozen dessert bars because they may contain egg yolk. People who have an allergy or severe sensitivity to eggs run the … [Read more...]

Filed Under: FDA Press Releases

Innovage Recalls Discovery Kids Lamps Due to Fire and Burn Hazards

July 4, 2012 By The CPSC Leave a Comment

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product. Name of … [Read more...]

Filed Under: CPSC Press Releases

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J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

509 Recalls Helmets Due to Risk of Head Injury

July 2, 2025 By The CPSC

SNLN Party Supply Toys Recalled Due to Ingestion Hazard; Risk of Serious Injury or Death; Federal Toy Standard Violation; Sold Exclusively on Amazon by Yiwu Dixikeji Douxiangongsi

July 2, 2025 By The CPSC

Harbor Freight Tools Recalls Predator 2000-Watt Power Stations Due to Shock Hazard

July 2, 2025 By The CPSC

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Jeriflyer Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment Hazard; Violation of the Virginia Graeme Baker Pool and Spa Safety Act; Sold on Amazon by Junjuanshop

July 2, 2025 By The CPSC

Positec Recalls Electric Corded Chainsaws and Pole Saws Due to Laceration Hazard

July 2, 2025 By The CPSC

Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Cefazolin for Injection Due to Product Mispackaging

June 27, 2025 By The FDA

Shang Hao Jia, Inc. Issues Allergy Alert on Undeclared Sesame in Danshi Brand Spicy Shredded Tofu

June 25, 2025 By The FDA

The Coleman Company Recalls Converta Camping Cots and Converta Camping Suspension Stretchers Due to Laceration and Amputation Hazards; Imported by Newell Brands

June 25, 2025 By The CPSC

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Shang Hao Jia, Inc. Issues Allergy Alert on Undeclared Sesame in Danshi Brand Spicy Shredded Tofu

June 25, 2025 By The FDA

The Coleman Company Recalls Converta Camping Cots and Converta Camping Suspension Stretchers Due to Laceration and Amputation Hazards; Imported by Newell Brands

June 25, 2025 By The CPSC

iHerb Recalls Bottles and Blister Packs of California Gold Nutrition Iron Supplements Due to Risk of Serious Injury or Death from Child Poisoning; Violation of Federal Standard for Child Resistant Packaging

June 25, 2025 By The CPSC

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-- See More Recall News

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