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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
May 13, 2026Food & BeverageFDA
Falcon Trading Co., Inc. recalls SunRidge Farms Organic SUNSET SOUP MIX CERTIFIED ORGANIC BY QAI NET WT. 25 LBS Item: 013000 UPC: 086700130001
Hazard: Potential contamination with pesticides, haloxyfop and thiamethoxam
May 13, 2026Food & BeverageFDA
Falcon Trading Co., Inc. recalls SunRidge Farms Organic CHILI BEAN BLEND CERTIFIED ORGANIC BY QAI NET WT. 15 LBS Item: 003056 UPC: 086700030561
Hazard: Potential contamination with pesticides, haloxyfop and thiamethoxam
May 13, 2026Food & BeverageFDA
Falcon Trading Co., Inc. recalls SunRidge Farms Organic Black Beans CERTIFIED ORGANIC BY QAI NET WT. 25 LBS. ORIGEN: ARGENTINA EXPORTADOR: ESPAR SRL FECH
Hazard: Potential contamination with pesticides, haloxyfop and thiamethoxam
May 13, 2026Food & BeverageFDA
Green Organic Vegetables recalls Woodstock Organic Shelled Edamame 10 oz. and 48 oz.
Hazard: Foreign object: metal pieces
May 13, 2026Food & BeverageFDA
Griffith Foods Inc. recalls MILK-N-EGG MIX NET WEIGHT: 50 LBS, PROCESSED FROM NONFAT DRIED MILK, DRIED WHEY, DRIED EGG WHITES CONTAINS: EGG, MILK Mf
Hazard: Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.
May 13, 2026Food & BeverageFDA
Griffith Foods Inc. recalls MILK WASH NET WEIGHT: 50OZ (1417g) Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta, GA 30349
Hazard: Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.
May 13, 2026Food & BeverageFDA
Griffith Foods Inc. recalls Costco Service Deli Department 63 MEATLOAF SEASONING MORE FLV Pack Size: 4-5lb. Bags Net Weight: 20lbs Allergy Informati
Hazard: Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.
May 13, 2026Food & BeverageFDA
Disaronno Ingredients S.p.a. recalls Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed 8 bags per master case of 2 Kg (4.41 lb) each total case weig
Hazard: Undeclared allergen Milk. The presence of the milk allergen in the product was found to exceed acceptable levels despite the product being labeled with the statement *May contain milk. *
May 13, 2026Food & BeverageFDA
SUNGAL INC recalls XZL, Jelly Snacks, 12.68 OZ, Bag. 12 Bags per Case.
Hazard: Product Contains undeclared FD&C Yellow #5 & #6 and Red #40
May 13, 2026Food & BeverageFDA
Tops Markets LLC recalls Christopher Ranch Peeled Garlic 6 oz.
Hazard: The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm
May 13, 2026Food & BeverageFDA
Tops Markets LLC recalls Garland Fresh Peeled Garlic 6 oz. bag
Hazard: The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm
May 13, 2026DrugsFDA
B BRAUN MEDICAL INC recalls Lactated Ringer's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0
Hazard: Presence of Particulate Matter.
May 13, 2026DrugsFDA
Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles recalls TPN bag (patient specific), Rx# 11-4909703-0-1, Compound Volume 1660 mL per bag, Rx only, Single Dose Injection, Refrige
Hazard: Incorrect Product Formulation: product did not contain insulin as listed in the label.
May 13, 2026DrugsFDA
Acella Pharmaceuticals, LLC recalls NAPROXEN ORAL SUSPENSION, USP, 125 mg/5mL, Rx only, 16fl oz (473 mL) bottles, Distributed by: Acella Pharmaceuticals, LL
Hazard: Chemical contamination; presence of lead and lithium above specification
May 13, 2026DrugsFDA
Breckenridge Pharmaceutical, Inc. recalls Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by Towa Pharmaceutical Eurpoe S.L., Marto
Hazard: CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit
May 13, 2026DrugsFDA
JB Chemicals and Pharmaceuticals Ltd recalls Enalapril Maleate Tablets, USP, 20 mg, 1,000-count bottle, Rx only, Manufactured by: Unique Pharmaceutical Laboratories
Hazard: Failed Impurities/Degradation Specifications:Out of specification result occurred in Organic Impurities Test
May 13, 2026DrugsFDA
Teva Pharmaceuticals USA, Inc recalls Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, In Single-Dose kits containing: 8-mL
Hazard: Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
May 13, 2026DrugsFDA
CareFusion 213, LLC recalls BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 0.36 fl
Hazard: Lack of assurance of Sterility: potential product contamination
May 13, 2026DrugsFDA
CareFusion 213, LLC recalls BD PurPrep, Povidone-iodine 8.3% w/w (0.83% available iodine) with isopropyl alcohol 72.5% w/w Sterile Solution, 25x26mL
Hazard: Lack of assurance of Sterility: potential product contamination
May 13, 2026DrugsFDA
Ajanta Pharma Ltd. recalls Duloxetine Delayed-Release Capsules, 20 mg, Rx Only, 60 capsules, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 0
Hazard: CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
May 13, 2026DrugsFDA
Ajanta Pharma Ltd. recalls Duloxetine Delayed-Release Capsules, 60 mg, Rx Only, 30 capsules, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 0
Hazard: CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
May 13, 2026DrugsFDA
Ajanta Pharma Ltd. recalls Duloxetine Delayed-Release Capsules, 30 mg, Rx Only, a) 90 Capsules, NDC 27241-098-09, b) 30 capsules, NDC 27241-098-03,
Hazard: CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
May 13, 2026DrugsFDA
Fresenius Medical Care Holdings, Inc. recalls DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 2
Hazard: Lack of Assurance of Sterility: Potential leaks from perforations in bags.
May 13, 2026DrugsFDA
Fresenius Medical Care Holdings, Inc. recalls DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only,
Hazard: Lack of Assurance of Sterility: Potential leaks from perforations in bags.
May 13, 2026DrugsFDA
Unichem Pharmaceuticals USA Inc. recalls busPIRone Hydrochloride Tablets, USP, 5 mg, 500-count bottle, Rx Only, Manufactured by Unichem Laboratories LTD., Ind, A
Hazard: Subpotent drug
May 13, 2026VehiclesNHTSA
Lucid 2024–2025 Electrical System recall
Hazard: A loss of drive power increases the risk of a crash.
May 13, 2026Vehicle EquipmentNHTSA
Weldon Equipment recall
Hazard: A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing the risk of injury.
May 12, 2026VehiclesNHTSA
Vespa 2026 Visibility recall
Hazard: Without the convex mirror warning, riders may misjudge the distance of other vehicles, resulting in unsafe lane changes or maneuvers, increasing the risk of a crash.
May 12, 2026VehiclesNHTSA
Lincoln, Ford 2026 Power Train recall
Hazard: A loss of park function can allow the vehicle to rollaway, increasing the risk of a crash.
May 12, 2026VehiclesNHTSA
Nova BUS 2019–2023 Structure recall
Hazard: A missing DOT code mark may result in the door being replaced with the incorrect type of plastic, reducing visibility and increasing the risk of a crash.