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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls C8-4v Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls C8-4v Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls C6-3 Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls C6-2 Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls C5-2 Lumify Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls C5-2 Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls c5-1 Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls C10-4ec Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls C10-3v Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls BP10-5ec Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls 7.5MHZ Endo Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls 3D9-3v Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Philips Ultrasound, Inc recalls 3D6-2 Transducer Probe
Hazard: To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
September 3, 2025Medical DevicesFDA
Tandem Diabetes Care, Inc. recalls Battery Operated infusion pumps. t:slim X2 G5, Replacement, Refurbished, REF: 1000911; t:slim X2 GS Classic, Replacemen
Hazard: Insulin pumps manufactured with speakers from Revision A and B may malfunction ("Malfunction 16") which prevents audible alerts and causes the pumps to become inoperable and stop infusing insulin which could result in a hyperglycemic event, which may lead to injury and/or hospitalization.
September 3, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE HealthCare OEC 9900 Elite C-arm Systems.
Hazard: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.
September 3, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE HealthCare OEC 9800.
Hazard: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user.
September 3, 2025Food & BeverageFDA
The J.M. Smucker Company recalls Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7 oz)
Hazard: Mold. The firm noticed an increase in customer complaints. They conducted a root cause investigation and discovered that one of their coolers had malfunctioning.
September 3, 2025Food & BeverageFDA
CHETAK NEW YORK LLC recalls Deep Sprouted Moong 16 oz
Hazard: Product tested positive Salmonella .
September 3, 2025Food & BeverageFDA
CHETAK NEW YORK LLC recalls Deep Sprouted Mat 16 oz.
Hazard: Product tested positive Salmonella .
September 3, 2025Food & BeverageFDA
Beaver Street Fisheries, Inc. recalls Great Value branded and Sea Best branded raw frozen shrimp in bulk packaging, master cartons. Master carton case is 20
Hazard: Product may be contaminated with Cesium-137 (Cs-137)
September 3, 2025Food & BeverageFDA
H & N Group Inc. recalls Frozen shrimp in bulk packaging. 20 lbs (10 x 2 lbs blocks); 20 lbs (20 x 1 lbs blocks); 9 lbs case UPC# SH0176; SH0430
Hazard: Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
September 3, 2025Food & BeverageFDA
Fromi Usa recalls Brie Royal Faucon; Net Weight about: 2.2lb/ 1kg LOT AUS/US
Hazard: Product may be contaminated with Listeria monocytogenes
September 3, 2025Food & BeverageFDA
Blue Bell Creameries, L.P. recalls Chocolate Chip Cookie Dough ice cream cartons with a Moo-llennium Crunch lid. Packaging contains Moo-llennium crunch.
Hazard: undeclared almond, walnut, and pecan.
September 3, 2025Food & BeverageFDA
NEW ACAI AMAZONAS LLC recalls Organic Mango Freeze Dried Powder, Bulk, 15-kilogram boxes (2 packs of 7.5 kilograms in a carton box), 7.5kg packaged in
Hazard: Potential Salmonella contamination
September 3, 2025Food & BeverageFDA
DFA Dairy Brands, LLC recalls Carton Label: "Friendly's Vanilla Bean"; 48 fl. oz. Lid Label: "Friendly's Cookies and Cream" Product in carton is Co
Hazard: Product contains undeclared wheat and soy.
September 3, 2025Food & BeverageFDA
Bakers Authority LLC recalls Baker's Authority Graham Cracker Meal; 5lb bag; stored dry at room temperature; packaged in silver bag
Hazard: Product label does not list ingredients including major food allergens: wheat and soy (vegetable oil). Additional undeclared ingredients include: niacin, reduced iron, vitamin B1, vitamin B2, invert sugar
September 3, 2025Food & BeverageFDA
Bakers Authority LLC recalls Baker's Authority Everything Bagel Mix; 5lb bag and 1lb bag; stored dry at room temperature; packaged in silver bag
Hazard: Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: poppy seeds, dried garlic, dried onion, and sea salt
September 3, 2025Food & BeverageFDA
Bakers Authority LLC recalls Baker's Authority Three Seed Mix; 5lb bag; stored dry at room temperature; packaged in silver bag
Hazard: Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: millet and flax
September 3, 2025Food & BeverageFDA
Martin Bauer, Inc. recalls Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic line
Hazard: Misbranding of the ingredient the firm sells ( Passionflower Herb Extract )
September 3, 2025Food & BeverageFDA
Breadbox Co. recalls Breadman Bakery; Multigrain 24oz. Baked for Breaman-Melrose Bakery Inc. UPC# 8 6000947952 4
Hazard: Finished product label does not include allergen ingredient Sesame Seed.