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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...]

      Winston Products Recalls 5/8-Inch HydroTech Expandable Burst-Proof Hoses Due to Risk of Impact Hazard and Temporarily Impaired Hearing

      The recalled hoses can burst, posing an impact hazard and a risk of temporarily impaired hearing. … [Read More...]

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Ruth’s Salad Charlotte NC is Recalling Ruth’s Original Pimento Spread 7 oz Because of Possible Health Risk. May Contain Listeria Monocytogenes

February 2, 2017 By The FDA Leave a Comment

Charlotte, NC Ruth’s Salads is undertaking a recall of Ruth’s Original Pimento Spread in 7oz plastic containers. The product has the potential to be contaminated with Listeria Monocytogenes. … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

Falafel King Issues Allergy Alert on Undeclared Milk in “Tzatziki Sauce”

February 2, 2017 By The FDA Leave a Comment

Falafel King of Boulder, Colorado is notifying the public that its containers of Tzatziki Sauce made with sour cream contains milk, a known allergen. People who have an allergy or severe sensitivity to milk run the risk of a serious or life-threatening allergic reaction if they consume these products. … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

Walt Disney Parks and Resorts Recalls Mickey Mouse Nightlights Due to Fire Hazard

February 2, 2017 By The CPSC Leave a Comment

… [Read more...]

Filed Under: CPSC Press Releases

Le Fedou, Fromagerie De Hyelzas Sas Recalls “Tomme Brebis Fedou Cheese” and “Soureliette Cheese” because of Possible Health Risk

February 1, 2017 By The FDA Leave a Comment

Fromi USA is recalling its 7 cases of Soureliette cheese and 2 cases of Tomme Brebis Fedou 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 … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

Barberi International Inc. Recalls Frozen Ajiaco Due to Possible Health Risk

February 1, 2017 By The FDA Leave a Comment

Barberi International Inc., based in Miami, Florida, is recalling its Sunmba Frozen Ajiaco (vegetable mix) product across Florida due to possible contamination with Listeria monocytogenes. Listeria monocytogenes is an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

U.S. Smokeless Tobacco Company Voluntarily Recalls Certain Smokeless Tobacco Products Manufactured at its Franklin Park, IL Facility

February 1, 2017 By The FDA Leave a Comment

U.S. Smokeless Tobacco Company (USSTC) is voluntarily recalling certain of its smokeless tobacco products, listed in the chart below, manufactured at USSTC’s facility in Franklin Park, IL. USSTC has notified the U.S. Food and Drug Administration of the recall and is working with federal authorities on this matter. USSTC initiated the recall after … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

Defective Smith & Nephew Tandem Bipolar Hip System

February 1, 2017 By US Recall News Leave a Comment

Specific batches of the Smith & Nephew tandem bipolar hip system have been recalled due to a defect that can cause the artificial hip joint to fall apart inside the patient’s body. When the implant fails, it is usually within the first few weeks of surgery. If your artificial hip comes apart, you will need revision surgery to remove and replace … [Read more...]

Filed Under: Bipolar Hip System

Defective Physiomesh Hernia Repair Patch

January 31, 2017 By US Recall News Leave a Comment

If you have suffered complications after ventral hernia repair, you may be a victim of the defective Ethicon Physiomesh Flexible Composite Mesh hernia patch. A ventral hernia is a bulge or hole in the abdominal wall often forming after a previous surgical incision doesn’t heal properly. Ethicon recalled its defective mesh in May, 2016, after … [Read more...]

Filed Under: Hernia Mesh

Heartburn Medicine Kidney Damage Lawsuits

January 31, 2017 By US Recall News Leave a Comment

If you have developed kidney problems after long-term use of heartburn medication, such as Nexium (esomeprazole) or Prilosec (omeprazole), your medication may be the culprit. Studies have found that long-term use of proton pump inhibitors (PPIs) increases the risk of kidney failure and chronic kidney disease. PPIs come in prescription form and are … [Read more...]

Filed Under: Proton Pump Inhibitors (PPIs)

New American Food Products, LLC Issues Allergy Alert on Weigels’s Mountain Valley and Royal Farms Market Place- Milk Chocolate Vanilla Caramels due to Undeclared Peanuts

January 31, 2017 By The FDA Leave a Comment

The recall was initiated due to concerns of the possible presence of peanuts. People who have an allergy or severe sensitivity to specific types of allergen, such as peanuts, run the risk of serious life threatening allergic reactions if they consume the product being recalled. … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

Defective Atrium C-Qur Surgical Mesh

January 30, 2017 By US Recall News Leave a Comment

Atrium C-Qur mesh is used in hernia repair, chest wall reconstruction, and in repairing traumatic and surgical wounds. The big selling point for C-Qur mesh is its omega 3 gel coating, derived from fish oil. The company even claims that the coating is, “all natural.” That sounds like a good thing but it may actually be the underlying problem in … [Read more...]

Filed Under: Uncategorized

NSE Products, Inc. Issues Allergy Alert on Undeclared Milk in Ageloc TR90 Protein Boost

January 28, 2017 By The FDA Leave a Comment

NSE Products, Inc. is recalling all ageLOC TR90 Protein Boost because it contains milk in the formula, which is not declared 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. … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

Marich Confectionery Co. Issues Allergy Alert On Potential Undeclared Almonds In Product

January 27, 2017 By The FDA Leave a Comment

Marich Confectionery of Hollister, California is voluntarily recalling 4.25oz Valentine Chocolate Caramel Hearts UPC CODE 797817-44440-9 because it may contain Triple Chocolate Toffee which contains almonds. People who have an allergy or severe sensitivity almonds run the risk of serious or life-threatening allergic reaction if they consume these … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

Fred Meyer Recalls Bakery Fresh Goodness Carrot Cupcakes Due to Undeclared Allergens

January 25, 2017 By The FDA Leave a Comment

Fred Meyer Stores has recalled Bakery Fresh Goodness Carrot Cupcakes sold in its retail stores because the product may contain milk and soy not listed on the label. … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

Carriage House Creations Recalls Carriage House Various Bourbon Basting Sauces and Hot Barbecue Sauce due to Undeclared Soy and Peanuts

January 25, 2017 By The FDA Leave a Comment

Carriage House Creations issues a voluntary product recall on all Bourbon Basting Sauces, and Hot Barbecue Sauce, due to undeclared soy and peanut ingredients found in the Worcestershire Sauce used in the making of these products. People, who have an allergy or severe sensitivity to soy or peanuts, run the risk of serious or life-threatening … [Read more...]

Filed Under: FDA Press Releases Tagged With: FDA, Recall

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J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Winston Products Recalls 5/8-Inch HydroTech Expandable Burst-Proof Hoses Due to Risk of Impact Hazard and Temporarily Impaired Hearing

July 23, 2025 By The CPSC

Curtis International Recalls Frigidaire-brand Minifridges Due to Fire and Burn Hazards; More Than $700,000 Reported in Property Damage

July 23, 2025 By The CPSC

Pura Scents Recalls Detachable Covers of Smart Home Fragrance Diffusers Due to Magnet Ingestion Hazard

July 23, 2025 By The CPSC

Hero Highlight

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

LED Gloves Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates the Mandatory Toy Standard and Child Resistant Coin Battery Packaging Standard; Sold on Amazon by Minongad

July 23, 2025 By The CPSC

Diamond G Forest Products Recalls Turpentine Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging

July 23, 2025 By The CPSC

Innovative Designs Recalls Minecraft Light-Up Slap Ruler Bracelets Due to Risk of Serious Injury or Death from Button Cell Battery Ingestion Hazard; Violates Mandatory Standard for Toys

July 23, 2025 By The CPSC

Creekwood Naturals Recalls 100% Natural Pure Gum Spirits of Turpentine Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging

July 23, 2025 By The CPSC

FENGQS Electric Bikes Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Sold on Amazon

July 23, 2025 By The CPSC

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Creekwood Naturals Recalls 100% Natural Pure Gum Spirits of Turpentine Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging

July 23, 2025 By The CPSC

FENGQS Electric Bikes Recalled Due to Fire and Burn Hazards; Risk of Serious Injury or Death; Sold on Amazon

July 23, 2025 By The CPSC

Aiho Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates Mandatory Standard; Sold on Walmart.com by Aiho

July 23, 2025 By The CPSC

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  • Winston Products Recalls 5/8-Inch HydroTech Expandable Burst-Proof Hoses Due to Risk of Impact Hazard and Temporarily Impaired Hearing
  • Curtis International Recalls Frigidaire-brand Minifridges Due to Fire and Burn Hazards; More Than $700,000 Reported in Property Damage
  • Pura Scents Recalls Detachable Covers of Smart Home Fragrance Diffusers Due to Magnet Ingestion Hazard
  • iMirror Inc. Recalls Electric Bug Zapper Racket, Fly Swatter, and Mosquito Swatter Due to Shock Hazard
  • Transpro US Recalls Electric Scooters with Unauthorized Lithium-Ion Battery UL Certification Labels Due to Fire and Burn Hazards; Risk of Serious Injury and Death; $200,000 in Property Damage Reported
  • LED Gloves Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates the Mandatory Toy Standard and Child Resistant Coin Battery Packaging Standard; Sold on Amazon by Minongad
  • Diamond G Forest Products Recalls Turpentine Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging
  • Innovative Designs Recalls Minecraft Light-Up Slap Ruler Bracelets Due to Risk of Serious Injury or Death from Button Cell Battery Ingestion Hazard; Violates Mandatory Standard for Toys
  • Creekwood Naturals Recalls 100% Natural Pure Gum Spirits of Turpentine Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging
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