Home / Recalls
Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
May 20, 2026Medical DevicesFDA
GE Medical Systems, LLC recalls Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15
Hazard: GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
May 20, 2026Medical DevicesFDA
GE Medical Systems, LLC recalls Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25
Hazard: GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
May 20, 2026Medical DevicesFDA
GE Medical Systems, LLC recalls Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23
Hazard: GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
May 20, 2026Medical DevicesFDA
GE Medical Systems, LLC recalls Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6
Hazard: GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
May 20, 2026Medical DevicesFDA
GE Medical Systems, LLC recalls Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300
Hazard: GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical convenience kits, containing Namic Manifold, Labeled as: TAVI, Medline Kit Number/SKU DYNJ904981C
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. MTS,RT,HANDED/LFT,HRT,KIT, Medline Kit Nu
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU DYN
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls 1. 3 VALVE MAN KIT, Medline Kit SKU Number: 65101544; 2. 3V MANIFOLD KIT, Medline Kit SKU Number: 65110351; 3. HEA
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls 1. DBD-MTS,3V,MAN,KIT, Medline Kit Number/SKU 60010195; 2. MTS-LEFT HEART,KIT, Medline Kit Number/SKU 60033123; 3. M
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107; Extravascular blood pressure transducer
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038402; Cardiopulmonary bypass adaptor, stopcock, mani
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038301; Cardiopulmonary bypass adaptor, stopcock, mani
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
Medline Industries, LP recalls Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, mani
Hazard: Medline has identified the presence of particulate within the fluid path of the Manifolds.
May 20, 2026Medical DevicesFDA
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN, W/COLDPAD, NS, RH Model/Catalog Number: 11-9099 Software Version: No Produc
Hazard: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
May 20, 2026Medical DevicesFDA
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Produc
Hazard: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
May 20, 2026Medical DevicesFDA
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,RH Model/Catalog Number: 11-1422 Software Version: no Produc
Hazard: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
May 20, 2026Medical DevicesFDA
DJO, LLC recalls Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product Desc
Hazard: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
May 20, 2026Medical DevicesFDA
On-X Life Technologies, Inc. recalls On-X Mitral Heart Valve with Conform-X Sewing Ring, Model: ONXMC-25/33
Hazard: Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.
May 20, 2026Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA S
Hazard: Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result in a loose connection or full disconnection between syringe and manifold. If unwinding occurs, there is a potential for biohazard exposure, blood loss, infection. or air embolism.
May 20, 2026Medical DevicesFDA
Omnicell, Inc. recalls Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRING
Hazard: Potential for mislabeled syringe produced by the i.v.STATION device.
May 20, 2026Food & BeverageFDA
Pure Ground Ingredients, Inc. recalls Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk; tea/food manufacturers. Closed container stored
Hazard: Product has the potential to be contaminated with Salmonella.
May 20, 2026Food & BeverageFDA
Sugar Foods LLC recalls Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ (141g) UPC 0 11110 81353 4 DISTRIBUTED BY THE KROGER CO., CINCIN
Hazard: Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella.
May 20, 2026Food & BeverageFDA
Ocinet, Inc. recalls ...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz U
Hazard: Undeclared allergen ingredient (fish)
May 20, 2026Food & BeverageFDA
Prospector Popcorn, LLC recalls Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar, corn syru
Hazard: Products contain undeclared soy, specifically soy lecithin.
May 20, 2026Food & BeverageFDA
Raja Foods and Vegetables Inc. recalls Swad Mango Flavored Masala Candy
Hazard: Contains undeclared Blue 1
May 20, 2026Food & BeverageFDA
Raja Foods and Vegetables Inc. recalls Swad Orange Flavored Masala Candy
Hazard: Contains undeclared FD&C Yellow 6
May 20, 2026Food & BeverageFDA
WE R NUTS recalls Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix, 11 oz Net Wt, packed in clear tamper resistant plastic container
Hazard: Contains undeclared allergens (cashews, milk, and soy).