Home / Recalls
Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
October 22, 2025Food & BeverageFDA
Black Sheep Egg Company, LLC recalls Free Range Grade AA Large White Eggs, 12ct Cartons, 15dz per box, Black Sheep Egg Company 400 S Memorial Drive Walnut
Hazard: Potential Salmonella contamination.
October 22, 2025Food & BeverageFDA
Black Sheep Egg Company, LLC recalls Free Range Grade AA Medium White Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive
Hazard: Potential Salmonella contamination.
October 22, 2025Food & BeverageFDA
Black Sheep Egg Company, LLC recalls Free Range Grade AA Large White Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive
Hazard: Potential Salmonella contamination.
October 22, 2025Food & BeverageFDA
Black Sheep Egg Company, LLC recalls Free Range Grade AA Medium Brown Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive
Hazard: Potential Salmonella contamination.
October 22, 2025Food & BeverageFDA
Black Sheep Egg Company, LLC recalls Free Range Grade AA Large Brown Eggs, Loose Open Skid, 900dz per pallet, Black Sheep Egg Company 400 S Memorial Drive
Hazard: Potential Salmonella contamination.
October 22, 2025Food & BeverageFDA
Black Sheep Egg Company, LLC recalls Free Range Grade AA Medium Brown Eggs, Loose Pack in Boxes, 15dz per box, Black Sheep Egg Company 400 S Memorial Drive
Hazard: Potential Salmonella contamination.
October 22, 2025Food & BeverageFDA
Black Sheep Egg Company, LLC recalls Free Range Grade AA Large Brown Eggs, Loose Pack in Boxes, 15dz per box, Black Sheep Egg Company 400 S Memorial Drive
Hazard: Potential Salmonella contamination.
October 22, 2025Food & BeverageFDA
Black Sheep Egg Company, LLC recalls Free Range Grade A Large Brown Eggs, 18ct Cartons, UPC: 860010568538, Black Sheep Egg Company 400 S Memorial Drive Wa
Hazard: Potential Salmonella contamination.
October 22, 2025Food & BeverageFDA
Black Sheep Egg Company, LLC recalls Free Range Grade A Large Brown Eggs, 12ct Cartons, UPC: 860010568507, Black Sheep Egg Company 400 S Memorial Drive Wal
Hazard: Potential Salmonella contamination.
October 22, 2025Food & BeverageFDA
Wawa Beverage Company recalls Wawa Strawberry Lemonade, 16 oz (Pint), Plastic bottle, Stored refrigerated, UPC: 007626191018982
Hazard: Potential foreign object contamination
October 22, 2025Food & BeverageFDA
Wawa Beverage Company recalls Wawa Strawberry Milk, Lowfat Milk, 16 oz (Pint), Plastic bottle, Stored refrigerated, UPC: 00726191015134
Hazard: Potential foreign object contamination
October 22, 2025Food & BeverageFDA
Wawa Beverage Company recalls Wawa HVD (Whole) Milk , 16 oz (Pint), Plastic bottle, Stored refrigerated, UPC: 00726191014403
Hazard: Potential foreign object contamination
October 22, 2025Food & BeverageFDA
ONE FROZEN, LLC recalls Good and Gather brand Southwest-Style Burrito Bowl Blend Processed in a facility that also handles shellfish, egg, fish
Hazard: Product may contain undeclared shrimp (crustacean shellfish).
October 22, 2025Food & BeverageFDA
Pacific Coast Producers recalls Pears Halves in Pear Juice from Concentrate; NET WT 15 OZ (425 g); Ingredients: Pears, Water, Pear Juice Concentrate; Di
Hazard: Potential contamination with heavy metal (Lead).
October 22, 2025Food & BeverageFDA
Pacific Coast Producers recalls Pears SLICED in Organic Pear Juice from Concentrate; NET WT 15 OZ (425 g); Ingredients: Organic Pears, Water, Organic Pe
Hazard: Potential contamination with heavy metal (Lead).
October 22, 2025Food & BeverageFDA
Pacific Coast Producers recalls Halved Pears IN PEAR JUICE FROM CONCNETRATE; NET WT 15 OZ (425 g); Ingredients: Pears, Water, Pear Juice Concentrate; Di
Hazard: Potential contamination with heavy metal (Lead).
October 22, 2025Food & BeverageFDA
Pacific Coast Producers recalls Fruit Cocktail IN 100% JUICE WITH ADDED INGREDIENTS; NET WT 15 OZ (425 g); Ingredients: Diced Peaches, Diced Pears, Wate
Hazard: Potential contamination with heavy metal (Lead).
October 22, 2025Food & BeverageFDA
Sea Port Products Corp recalls Sea Port brand, Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo size 16-20. Product of Indonesia. Distributed
Hazard: Shrimp may be contaminated with Cesium-137 (Cs-137).
October 22, 2025Food & BeverageFDA
Garden Fresh Foods, Inc. recalls Sliced (1/4") green onions, refrigerated, packaged in plastic bag. Each case consist 5/6lbs. bag (net wt. 30lbs.). Garde
Hazard: Possible positive Listeria monocytogenes. Firm tested one lot of sliced green onions in-house and found Listeria monocytogenes.
October 22, 2025Food & BeverageFDA
Now Foods recalls NOW Real Food Organic Unsalted Whole Raw Cashews, 10 oz. pouch, UPC 7 33739 07066 1 Product Code 7066
Hazard: Undeclared pine nut
October 22, 2025Food & BeverageFDA
D & M Smoked Fish, Inc. recalls Haifa COLD SMOKED SEABASS 8 OZ
Hazard: Contaminated with Listeria monocytogenes
October 22, 2025Food & BeverageFDA
D & M Smoked Fish, Inc. recalls Haifa COLD SMOKED SALMON 8 OZ.
Hazard: Contaminated with Listeria monocytogenes
October 22, 2025DrugsFDA
Rising Pharma Holding, Inc. recalls Carbidopa, Levodopa, Entacapone Tablets, 25 mg/100 mg/200 mg, 100-count bottle, Rx Only, Manufactured for: Rising Pharma
Hazard: Product mix up: complaint received that sealed medication bottle contained Carbidopa, Levodopa, and Entacapone film-coated tablets (37.5 mg/150 mg/200 mg) instead of labelled lower strength Carbidopa, Levodopa, and Entacapone film-coated tablets (25 mg/100 mg/200 mg).
October 22, 2025DrugsFDA
ASTRAZENECA PHARMACEUTICALS recalls Fasenra (benralizumab) Injection, 30 mg/mL, one single-dose pre-filled syringe, Rx only, Manufactured by: AstraZeneca AB
Hazard: Lack of Assurance of Sterility:
October 22, 2025DrugsFDA
Amerisource Health Services LLC recalls Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio
Hazard: CGMP Deviations: The recalling firm filed for Chapter 11 on September 30, 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
October 22, 2025DrugsFDA
Endo USA, Inc. recalls Everolimus tablets 5mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by
Hazard: Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
October 22, 2025DrugsFDA
STAQ Pharma, Inc. recalls FentaNYL Citrate PF, 500mcg/50 mL (10mcg/mL) in NACL, Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42n
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date
October 22, 2025DrugsFDA
STAQ Pharma, Inc. recalls Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, De
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date
October 22, 2025DrugsFDA
STAQ Pharma, Inc. recalls Hydromorphone HCL PF, 10mg/50 mL (0.2mg/mL) in NACL, Injection for IV use, 50 mL Syringe, STAQ Pharma Inc., 14135 E 42nd
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date
October 22, 2025DrugsFDA
SV Labs Prescott Corporation recalls Aloe Up Sport Performance Sunscreen Lotion SPF 30, 1 FL OZ (30 mL) per tube, Mfd. for: ALOE UP, 9700 W. 76th St., Ste 11
Hazard: cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing.