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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...]

      Hartford Bakery, Inc. Issues Allergy Alert on Undeclared Hazelnuts in “Lewis Bake Shop Artisan Style ½ Loaf”

      Summary Company Announcement Date: July 10, 2025 FDA Publish Date: July … [Read More...]

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Kermit, Inc. Issues Allergy Alert on Undeclared Soy and Anchovies in Various Barbecue Sauces

January 11, 2016 By The FDA Leave a Comment

Kermit, Inc. of DeLand, Florida is recalling products co-packed for Peddlin' Rooster, P.O. Box 1743, DeLand, Florida 32721, because of an undeclared allergen on the label. The undeclared allergen is soy and anchovies as a ingredient in Reduced Sodium Worcestershire Sauce and Organic Ketchup that is used in making of several products. … [Read more...]

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

Good Earth Egg Company Voluntarily Recalls Shell Eggs Because Of Possible Health Risk

January 9, 2016 By The FDA Leave a Comment

Good Earth Egg Company, LLC of Bonne Terre, Missouri has announced a voluntary recall of its shell eggs because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected … [Read more...]

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

R Thomas Marketing LLC In Conjunction With Just Enhance LLC Issues Nationwide Recall Of Black Ant, Herb Viagra, Real Skill, Weekend Prince, African Black Ant And Stree Overlord Along With Multiple Other Products Due To Undeclared Sildenafil

January 9, 2016 By The FDA Leave a Comment

R Thomas Marketing LLC is voluntarily recalling all lots of several products to the consumer level. These products by Black Ant, Herb Viagra, Real Skill, Stree Overlord, Weekend Prince, and African Black Ant were tested by the FDA and found to contain Sildenafil, a PDE-5 Inhibitor which is the active ingredient in an FDA-approved drug for erectile … [Read more...]

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

New York Style Sausage Co. Recalls Pork Products Due To Misbranding

January 8, 2016 By The USDA Leave a Comment

New York Style Sausage Co., a Sunnyvale, Calif. establishment, is recalling approximately 4,040 pounds of pork sausage products due to misbranding. The products are encased in sheep casings, which are not declared on the product label. … [Read more...]

Filed Under: USDA Press Releases Tagged With: Food Recall

Shakti Group USA LLC Recalls L.G Compounded Asafoetida Powder Because Of Possible Health Risk

January 8, 2016 By The FDA Leave a Comment

Shakti Group USA LLC of New Brunswick, NJ is recalling 50 gm and 100 gm sizes of L.G Compounded Asafoetida Powder, both coded with Lot Number: 2323 because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened … [Read more...]

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

Giant Eagle Youngstown Voluntarily Recalls New Year's Pretzels from Select Stores Due to an Undeclared Walnut Allergen

January 7, 2016 By The FDA Leave a Comment

All lots of Giant Eagle brand New Year's Pretzels prepared and sold individually from the Bakery department inside the Niles Giant Eagle at 48 Vienna Avenue in Niles, Ohio since December 26 have been voluntarily recalled by Giant Eagle due to an undeclared walnut allergen. People who have an allergy or severe sensitivity to walnuts run the risk of … [Read more...]

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

Giant Eagle Pittsburgh Voluntarily Recalls New Year's Pretzels from Select Stores Due to an Undeclared Walnut Allergen

January 7, 2016 By The FDA Leave a Comment

All lots of Giant Eagle brand New Year's Pretzels prepared and sold individually from the Bakery department inside select Giant Eagle and Market District supermarkets since December 26 have been voluntarily recalled by Giant Eagle due to an undeclared walnut allergen. People who have an allergy or severe sensitivity to walnuts run the risk of a … [Read more...]

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

Giant Eagle Cleveland Voluntarily Recalls New Year's Pretzels from Select Stores Due to an Undeclared Walnut Allergen

January 7, 2016 By The FDA Leave a Comment

All lots of Giant Eagle brand New Year's Pretzels prepared and sold individually from the Bakery department inside select Giant Eagle and Market District supermarkets since December 26 have been voluntarily recalled by Giant Eagle due to an undeclared walnut allergen. People who have an allergy or severe sensitivity to walnuts run the risk of a … [Read more...]

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

Market District Voluntarily Recalls New Year's Pretzels Due to an Undeclared Walnut Allergen

January 7, 2016 By The FDA Leave a Comment

All lots of New Year's Pretzels prepared and sold individually from the Bakery department inside the Carmel Market District located at 11505 N Illinois Street in Carmel, Indiana since December 26 have been voluntarily recalled by Giant Eagle, Inc. due to an undeclared walnut allergen. People who have an allergy or severe sensitivity to walnuts run … [Read more...]

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

Milky Way International Trading Corp. Issues Voluntary Nationwide Recall of Nice! Mandarin Oranges in 8-ounce Bottles Due to Possible Glass in Products

January 7, 2016 By The FDA Leave a Comment

Milky Way International Trading Corp. today announced the recall of Nice! Mandarin Oranges in 8-ounce bottles due to potential glass in the product. The affected product was distributed to Walgreens stores nationwide and displays one of the lot numbers listed below. Consumers could potentially be cut or injured if ingested. To date there have been … [Read more...]

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

Cape Cod Provisions LLC Issues Allergy Alert on Undeclared Almonds in Product

January 7, 2016 By The FDA Leave a Comment

Cape Cod Provisions LLC of Pocasset, MA is recalling Cape Cod Cranberry Candy and Harvest Sweets Milk Chocolate/Dark Chocolate/Yogurt Covered Cranberry Blend (mix of all three varieties in the package) because they may contain undeclared yogurt covered almonds. These products can further be identified by their UPC codes; Cape Cod Cranberry Candy … [Read more...]

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

Zulily Recalls Children’s Pajamas Due to Violation of Federal Flammability Standard (Recall Alert)

January 7, 2016 By The CPSC Leave a Comment

The pajamas do not meet the federal flammability standards for children’s sleepwear, posing a risk of burn injuries. … [Read more...]

Filed Under: CPSC Press Releases

Office Depot Recalls Executive Chairs Due to Fall Hazard

January 7, 2016 By The CPSC Leave a Comment

The seat plate weld can break, posing a fall hazard to consumers. … [Read more...]

Filed Under: CPSC Press Releases

Neto's Sausage Co., Inc. Recalls Meat and Poultry Products Produced Without Benefit of Inspection

January 6, 2016 By The USDA Leave a Comment

Neto's Sausage Co., Inc, a Santa Clara, Calif., establishment, is recalling approximately 7,687 pounds of beef, pork, and chicken products that were produced and labeled with the federal mark of inspection without the benefit of FSIS inspection. … [Read more...]

Filed Under: USDA Press Releases Tagged With: Food Recall

Hospira Issues a Voluntary Nationwide Recall of One Lot of Magnesium Sulfate in Water for Injection Due to Incorrect Barcode Labeling on the Primary Container

January 5, 2016 By The FDA Leave a Comment

Hospira, Inc., a Pfizer company, has announced a voluntary recall of one lot of, MAGNESIUM SULFATE IN WATER FOR INJECTION (0.325 mEq Mg**/mL) 40 mg/mL 2g total, 50 mL (NDC: 0409-6729-24, Lot 53-113-JT, Expiry 1NOV2016) to the user level due to a confirmed customer report of an incorrect barcode on the primary bag labeling. The product has a barcode … [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

Hartford Bakery, Inc. Issues Allergy Alert on Undeclared Hazelnuts in “Lewis Bake Shop Artisan Style ½ Loaf”

July 10, 2025 By The FDA

Wiet Peeters Farm Products Limited RECALLS “Aunt Mid’s Fresh Sliced Mushrooms, Peeters Mushroom Farm Cremini Sliced and Peeters Mushroom Farm Thick Slice Mushroom ” Because of Possible Listeria Monocytogenes Contamination

July 10, 2025 By The FDA

Walmart Recalls Ozark Trail 64 oz Water Bottles Due to Serious Impact and Laceration Hazards

July 9, 2025 By The CPSC

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J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

SPPTTY Kids Bicycles Recalled Due to Risk of Death or Injury from Lead Poisoning; Violates Federal Lead Content Ban; Sold at Walmart by Shenzhen Yihuachuang Technology

July 9, 2025 By The CPSC

AUGNORYE Padded Crib Bumpers Recalled Due to Risk of Serious Injury or Death from Suffocation; Violates Federal Crib Bumper Ban; Sold on Amazon by YIXIA

July 9, 2025 By The CPSC

Braided Crib Bumpers Recalled Due to Risk of Serious Injury or Death from Suffocation; Violates Federal Crib Bumper Ban; Sold on Amazon by Haoyunm

July 9, 2025 By The CPSC

Creekliybear Play Yard Mattresses Recalled Due to Risk of Serious Injury or Death from Entrapment Hazard; Violates Mandatory Standard for Crib Mattresses; Sold on Amazon by Kbabyea

July 9, 2025 By The CPSC

Dearlomum Retractable Safety Gates Recalled Due to Risk of Serious Injury or Death to Children from Entrapment Hazard; Violates Federal Standard for Gates and Enclosures; Sold on Amazon by Signbaby

July 9, 2025 By The CPSC

J&J Settles Talc Mesothelioma Settlement

January 15, 2020 By Advice Media

Creekliybear Play Yard Mattresses Recalled Due to Risk of Serious Injury or Death from Entrapment Hazard; Violates Mandatory Standard for Crib Mattresses; Sold on Amazon by Kbabyea

July 9, 2025 By The CPSC

Dearlomum Retractable Safety Gates Recalled Due to Risk of Serious Injury or Death to Children from Entrapment Hazard; Violates Federal Standard for Gates and Enclosures; Sold on Amazon by Signbaby

July 9, 2025 By The CPSC

CHS Inc. Recalls Payback Champion Lamb Feed Due to Elevated Copper Health Risk

July 9, 2025 By The FDA

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Recent Posts

  • Hartford Bakery, Inc. Issues Allergy Alert on Undeclared Hazelnuts in “Lewis Bake Shop Artisan Style ½ Loaf”
  • Wiet Peeters Farm Products Limited RECALLS “Aunt Mid’s Fresh Sliced Mushrooms, Peeters Mushroom Farm Cremini Sliced and Peeters Mushroom Farm Thick Slice Mushroom ” Because of Possible Listeria Monocytogenes Contamination
  • Walmart Recalls Ozark Trail 64 oz Water Bottles Due to Serious Impact and Laceration Hazards
  • WLIVE Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violations of Federal Standard for Clothing Storage Units; Sold on Amazon by WLIVE
  • Giant Bicycle Recalls Momentum Vida E+ E-Bikes Due to Crash Hazard
  • SPPTTY Kids Bicycles Recalled Due to Risk of Death or Injury from Lead Poisoning; Violates Federal Lead Content Ban; Sold at Walmart by Shenzhen Yihuachuang Technology
  • AUGNORYE Padded Crib Bumpers Recalled Due to Risk of Serious Injury or Death from Suffocation; Violates Federal Crib Bumper Ban; Sold on Amazon by YIXIA
  • Braided Crib Bumpers Recalled Due to Risk of Serious Injury or Death from Suffocation; Violates Federal Crib Bumper Ban; Sold on Amazon by Haoyunm
  • Creekliybear Play Yard Mattresses Recalled Due to Risk of Serious Injury or Death from Entrapment Hazard; Violates Mandatory Standard for Crib Mattresses; Sold on Amazon by Kbabyea
-- See More Recall News

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