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Consumer Product Recalls
127,502 recalls from the U.S. Consumer Product Safety Commission, newest first.
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201806 RASPBERRY FILLED DONUT 78x2.75OZ, NET WT 12.07 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201805 APPLE FRITTER 60x2.5 OZ, NET WT 8.44 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201804 Yeast Ring Donut 108x2.15OZ, NET WT 13.06 LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201780 GEN CHOC CK DONUT RINGS PFD 90x2.5OZ, NET WT12.66LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
FGF, LLC recalls item 8201779 GEN PLN CAKE DONUT RINGS PFD 90x2.5 OZ, NET WT 12.66LB
Hazard: potential for contamination with listeria monocytogenes
February 12, 2025Food & BeverageFDA
Dierbergs Markets, Inc. recalls Dierbergs Kitchen 16 oz Mac & Cheese packaged in a black plastic container with a clear plastic lid with a white label,
Hazard: Undeclared allergens (wheat) on label, incorrect label was placed on product
February 12, 2025Food & BeverageFDA
Vidaslim Co. recalls VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and Root Capsu
Hazard: Due to the presence of Toxic yellow oleander
February 12, 2025Food & BeverageFDA
Atkinson Milling Company recalls ATKINSON'S NO ONIONS PLAIN NO ONIONS HUSHPUPPIES NET WT. 2 LB. 8 OZ. UPC 0 72119 20304 7 Ingredients: Enriched Whole Gra
Hazard: Undeclared Milk. During the firm's reordering process of labels, they discovered that the label does not list milk in its ingredient or contain statement.
February 12, 2025Food & BeverageFDA
Atkinson Milling Company recalls ATKINSON'S HUSHPUPPIES WITH ONIONS NET WT. 1LB. (454 g) UPC 0 72119 20718 2 and NET WT. 2 LB. 8 OZ. UPC 0 72119 20305 4
Hazard: Undeclared Milk. During the firm's reordering process of labels, they discovered that the label does not list milk in its ingredient or contain statement.
February 12, 2025Food & BeverageFDA
Pecan Star & Nut Corp. recalls Greenwise Organic Pecan Halves 8 ounce, plastic printed package marked with lot # 18228 and with a best by date of April
Hazard: Undeclared walnuts
February 12, 2025Food & BeverageFDA
Middle East/ Soli's Baking Company, Inc. dba Middle East Baking Co. recalls CAIRO BAKERY PITA POCKET BREAD TRADITIONAL RECIPE EXTRA LARGE 6 COUNT, NET WT. 16 OZ. (1 lb.) (454g)
Hazard: Undeclared milk
February 12, 2025Food & BeverageFDA
Bazzini LLC recalls NuGo Dark Pretzel/Chocolate Chip Multipack 18 ct., 50g bar, 18 bars/tray, 9 trays/case. 40case/pallet
Hazard: The product is being recalled because of undeclared milk .
February 12, 2025Food & BeverageFDA
Bazzini LLC recalls NuGo Dark Chocolate Chip, Real Dark Chocolate / Vegan. 12g Protein
Hazard: The product is being recalled because of undeclared milk .
February 12, 2025Food & BeverageFDA
Bazzini LLC recalls NuGo Dark Chocolate Pretzel with Sea Salt , Real Dark Chocolate / Vegan. 12g Protein
Hazard: The product is being recalled because of undeclared milk .
February 12, 2025Food & BeverageFDA
Monkey Spit recalls Monkey Spit "Monkey Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Manufactu
Hazard: Barbeque sauce product contains undeclared listing of (Milk) in product ingredient listing from sub-ingredient Butter.
February 12, 2025Food & BeverageFDA
Monkey Spit recalls Monkey Spit "Atomic Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Manufactu
Hazard: Barbeque sauce product contains undeclared allergen listing of (Milk) in product ingredient listing from sub-ingredient Butter.
February 12, 2025Food & BeverageFDA
Monkey Spit recalls Monkey Spit "Swamp Mop" BBQ Sauce, 12 fl oz (355ml) glass bottle, 12 bottles/case; Refrigerate after opening; Monkey Spi
Hazard: Barbeque sauce product contains undeclared allergens (soy) contained in sub-ingredient
February 12, 2025DrugsFDA
ENDO USA, Inc. recalls Adrenalin Chloride Solution (Epinephrine Nasal Solution, USP), 30mg/30mL (1mg/mL), packaged in 30 mL vials, Distributed
Hazard: Labeling: Not Elsewhere Classified: misleading label similar in appearance to the FDA-approved drug product Adrenalin¿ (epinephrine injection, USP)
February 12, 2025DrugsFDA
PAI Holdings, LLC. dba Pharmaceutical Associates Inc recalls Guaifenesin and Codeine Phosphate Oral Solution USP, 100mg/10 mg per 5 mL, 16 fl oz (473 ml) bottles, PAI Pharmaceutical
Hazard: Superpotent; sodium benzoate preservative
February 12, 2025DrugsFDA
The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recalls Potassium Chloride Extended-Release Tablets, USP, 10 mEq (750 mg), 100 Tablets per carton (10 x 10 unit dose blisters),
Hazard: Failed Dissolution Specifications.
February 12, 2025DrugsFDA
SKY PACKAGING recalls HydrALAZINE Hydrochloride, 100 Tablets (10x10), USP, 50mg, Rx only, Manufactured by Strides Pharma Science Ltd, Bengalur
Hazard: Failed Impurities/Degradation Specifications
February 12, 2025DrugsFDA
SKY PACKAGING recalls HydrALAZINE Hydrochloride, 25 mg, 100 Unit Dose Tablets (10x10), USP, Rx only, Manufactured by Strides Pharma Science Lt
Hazard: Failed Impurities/Degradation Specifications
February 12, 2025DrugsFDA
Teva Pharmaceuticals USA, Inc recalls Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL, Single Dose prefilled syringe, packaged as a) 1 syringe in 1 CARTON, N
Hazard: Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit
February 12, 2025DrugsFDA
RemedyRepack Inc. recalls Carvedilol 25 mg Tablet, QTY: 30 Tablets per Blister Pack (3 x 10 blister cards), Rx Only, MFG by: Glenmark, Mahwah, NJ
Hazard: CGMP deviations: presence of N-Nitroso Carvedilol Impurity-1 (NNC 1), above the FDA recommended acceptable intake limit.
February 12, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Carvedilol Tablets, USP, 12.5 mg, Rx only, a)500 Tablets, NDC 68462-164-05; b) 100 Tablets, NDC 68462-164-01, Manufactur
Hazard: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit.
February 12, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Carvedilol Tablets, USP, 25 mg, Rx only, a)500 Tablets, NDC 68462-165-05; b) 100 Tablets, NDC 68462-165-01, Manufactured
Hazard: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit.
February 12, 2025DrugsFDA
FDC Limited recalls Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Auran
Hazard: Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
February 12, 2025VehiclesNHTSA
Volkswagen, Audi 2022–2025 Back Over Prevention recall
Hazard: A rearview camera that does not display an image can reduce the driver's rear view, increasing the risk of a crash.
February 12, 2025VehiclesNHTSA
Volkswagen 2025 Power Train recall
Hazard: A sudden loss of drive power can increase the risk of a crash.
February 12, 2025VehiclesNHTSA
Audi 2021–2024 Electrical System recall
Hazard: A high-voltage battery that overheats increases the risk of a fire.