Home / Recalls
Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
June 18, 2025Food & BeverageFDA
Sysco Corporation recalls 3909520 2/5# IMPERIAL FRESH CUCUMBER DICED 3/8 SK-ON ALL LOT CODES 480414 2/5 # IMPERIAL FRESH FC CUCUMBER STRIPED AND S
Hazard: Cucumbers have the potential to be contaminated with Salmonella
June 18, 2025Food & BeverageFDA
Unilever Manufacturing (US), Inc. recalls Rocky Road Ice Cream packaged in a Breyer Chocolate Truffle Tub that says "may contain tree nuts" with a Breyers Rocky R
Hazard: Undeclared allergens and mislabeled product. Rocky Road Ice was packaged with Chocolate Truffle Ice Cream labeled tub and a Rocky Road Ice Cream lid. Tub said "may contain tree nuts" the lid said it did contain almonds.
June 18, 2025Food & BeverageFDA
COMVITA USA INC recalls Comvita branded Manuka Honey + Reishi; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode# 658196001013
Hazard: Leaking induction seal on packaging.
June 18, 2025Food & BeverageFDA
COMVITA USA INC recalls Comvita branded Manuka Honey + Cordyceps for energy; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode# 658196001037
Hazard: Leaking induction seal on packaging.
June 18, 2025Food & BeverageFDA
COMVITA USA INC recalls Comvita branded Manuka Honey + Lion's Mane for Focus; made in New Zealand, Net Wt. 12 fl oz (355g); Barcode# 65819600102
Hazard: Leaking induction seal on packaging.
June 18, 2025Food & BeverageFDA
Vern's Foods & Farm recalls Taylor Shellfish Farms Geoduck Chowder Base, frozen, Ingredients: Potatoes, Clam (Geoduck) ***Butter (Cream, Salt), Fish
Hazard: The ingredients statement declares fish sauce but does not declare anchovies. The Contains statement does not declare fish (anchovies).
June 18, 2025Food & BeverageFDA
Now Foods recalls NOW Nutritional Yeast Powder, Nt. Wt. 10oz. UPC 7 33739 02460 2
Hazard: regular yeast was inadvertently packaged as nutritional yeast
June 18, 2025Food & BeverageFDA
R&M TRADING LLC recalls Instant Milk Tea Brown Sugar Flavor, R&M Refresher brand, B0D725TXQW, net wt. 1lb. Product is sold in 3-pack. Parent A
Hazard: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
June 18, 2025Food & BeverageFDA
R&M TRADING LLC recalls Instant Milk Tea Original Flavor, R&M Refresher brand, B0D71YHZX4, net wt. 1lb. Product is sold in 1-pack or 3-pack. Pa
Hazard: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
June 18, 2025Food & BeverageFDA
R&M TRADING LLC recalls Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y85TG, net wt. 1lb. Product was sold in 1-pack or 3-pack. Par
Hazard: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
June 18, 2025Food & BeverageFDA
R&M TRADING LLC recalls Instant Milk Tea Taro Flavor, R&M Refresher brand, B0D72CMLBH, net wt. 1lb. Product was sold in 1-pack or 3-pack. Pare
Hazard: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
June 18, 2025Food & BeverageFDA
R&M TRADING LLC recalls Instant Milk Tea Honeydew Flavor, R&M Refresher brand, B0D7269JC1, net wt. 1lb. Product was sold in 1-pack or 3-pack.
Hazard: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
June 18, 2025Food & BeverageFDA
NRC Nutrition Pty Ltd recalls Preconception Multi for Women 60 capsules packaged in blister packs Batch 42469
Hazard: inconsistent blending of iodine in the product
June 18, 2025Food & BeverageFDA
Sweetheart USA, LLC recalls Gluten Free Vegan Peanut Butter Jam Cookie, Net Wt. 3.5 oz (200g), packaged individually in plastic
Hazard: Undeclared sesame
June 18, 2025DrugsFDA
Zydus Pharmaceuticals (USA) Inc recalls Icosapent Ethyl Capsules 1 gram, 120 Capsules per Bottle, Rx Only, Manufactured by Doppel Farmaceutici s.r.l., Piacenza,
Hazard: Failed Tablet/Capsule specifications; a product complaint was reported for burnt or melted capsules. This was determined to be a result of oxidation by leakage of capsule contents.
June 18, 2025DrugsFDA
Amneal Pharmaceuticals, LLC recalls Sulfamethoxazole and Trimethoprim Tablets, USP, 400 mg/80 mg, Rx Only, a) 100 Tablets per Bottle, NDC: 65162-271-10, b)
Hazard: Microbial contamination of non-sterile products: tablets may exhibit black spots due to microbial contamination.
June 18, 2025DrugsFDA
Macleods Pharmaceuticals Ltd recalls Levothyroxine Sodium Tablets, USP 112 mcg (0.112mg), 1000 tablets, Rx Only, Manufactured for: Macleods Pharma USA, Inc.
Hazard: Presence of a foreign substance: black hair found embedded in tablet.
June 18, 2025DrugsFDA
Ascend Laboratories, LLC recalls Cephalexin for Oral Suspension, USP, 125 mg per 5 mL, 200 mL (when mixed), Rx Only, Manufactured by: Alkem Laboratories
Hazard: Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.
June 18, 2025DrugsFDA
Ascend Laboratories, LLC recalls Cephalexin for Oral Suspension, USP, 125 mg per 5 mL, 100 mL (when mixed), Rx Only, Manufactured by: Alkem Laboratories
Hazard: Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.
June 18, 2025DrugsFDA
SAINI TRADE INC recalls Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.
Hazard: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
June 18, 2025DrugsFDA
SAINI TRADE INC recalls ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, U
Hazard: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
June 18, 2025DrugsFDA
SAINI TRADE INC recalls ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.
Hazard: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil.
June 18, 2025DrugsFDA
SAINI TRADE INC recalls MALEXTRA, Recharge with Extra, Dietary Supplement, 10 capsules per box, Distributed by: Health Fixer, Tempe, AZ 85288, U
Hazard: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
June 18, 2025DrugsFDA
SAINI TRADE INC recalls Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, U
Hazard: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
June 18, 2025DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Ezetimibe and Simvastatin Tablets, 10mg/40mg, 90-count bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd.,
Hazard: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for related substances test for Anhydro Simvastatin at the 06-month time point during long-term stability study.
June 18, 2025DrugsFDA
AvKARE recalls Chlorthalidone Tablets, USP, 25 mg, 50 Tablets (5x10) Unit Dose cards per carton, Rx only, Manufactured for: AvKARE, Pul
Hazard: Failed Dissolution Specifications
June 18, 2025DrugsFDA
AvKARE recalls Celecoxib Capsules, 200 mg, 50 Capsules (5x10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Pulaski, TN 3847
Hazard: Presence of Foreign Tablets/Capsules: manufacturer recalled because one tadalafil 5mg tablet was found in 500 count bottle of Celecoxib 200 mg capsules
June 18, 2025DrugsFDA
Alembic Pharmaceuticals Limited recalls Celecoxib Capsules, 200 mg, 500-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Div
Hazard: Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil 5mg tablet inside a sealed 500-count bottle of Celecoxib 200mg capsule
June 18, 2025VehiclesNHTSA
Mazda 2025 Engine And Engine Cooling recall
Hazard: Shifting into gear without the brake pedal depressed can result in unexpected vehicle movement, increasing the risk of a crash.
June 18, 2025VehiclesNHTSA
Holiday Rambler, Fleetwood 2025–2026 Equipment recall
Hazard: A faulty CO or LP detector may not notify occupants of carbon monoxide or propane exposure, increasing the risk of injury or death.