Recalls — last 90 days
- 2026-05-20FDA-DeviceGE Medical Systems, LLCClass IIGE Revolution Apex CT scanner security vulnerability
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.
- 2026-05-20FDA-DeviceGE Medical Systems, LLCClass IIGE Revolution CT ES recalled for security vulnerability
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.
- 2026-05-20FDA-DeviceGE Medical Systems, LLCClass IIGE Revolution Apex Plus CT recalled for security vulnerability
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.
- 2026-05-20FDA-DeviceGE Medical Systems, LLCClass IIGE Revolution Apex Elite CT scanner has security vulnerability
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.
- 2026-05-20FDA-DeviceGE Medical Systems, LLCClass IIGE Revolution CT recalled for software security vulnerability
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.
- 2026-05-20FDA-DeviceMedline Industries, LPClass IMedline TAVI kits recalled for particulate contamination
Medline has identified the presence of particulate within the fluid path of the Manifolds.
- 2026-05-20FDA-DeviceMedline Industries, LPClass IMedline cardiac kits recalled for particulate contamination
Medline has identified the presence of particulate within the fluid path of the Manifolds.
- 2026-05-20FDA-DeviceMedline Industries, LPClass IMedline cardiac manifold kits recalled for particulate contamination
Medline has identified the presence of particulate within the fluid path of the Manifolds.
- 2026-05-20FDA-DeviceMedline Industries, LPClass IMedline catheter lab kits recalled for particulate contamination
Medline has identified the presence of particulate within the fluid path of the Manifolds.
- 2026-05-20FDA-DeviceMedline Industries, LPClass IMedline Namic Preceptor manifold recalled for particulate contamination
Medline has identified the presence of particulate within the fluid path of the Manifolds.
- 2026-05-20FDA-DeviceMedline Industries, LPClass IMedline Namic Preceptor manifold recalled for particulate contamination
Medline has identified the presence of particulate within the fluid path of the Manifolds.
- 2026-05-20FDA-DeviceMedline Industries, LPClass IMedline Namic Angiographic Manifold recalled for particulate contamination
Medline has identified the presence of particulate within the fluid path of the Manifolds.
- 2026-05-20FDA-DeviceMedline Industries, LPClass IMedline Namic Angiographic Manifold recalled for particulate contamination
Medline has identified the presence of particulate within the fluid path of the Manifolds.
- 2026-05-20FDA-DeviceMedline Industries, LPClass IMedline Namic Angiographic Manifold recalled for particulate contamination
Medline has identified the presence of particulate within the fluid path of the Manifolds.
- 2026-05-20FDA-DeviceDJO, LLCClass IIDJO IceMan cold therapy unit recalled for connector failure
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
- 2026-05-20FDA-DeviceDJO, LLCClass IIDJO DONJOY IceMan CLASSIC3 recalled for broken connector
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
- 2026-05-20FDA-DeviceDJO, LLCClass IIDJO DONJOY ICEMAN cold therapy unit recalled for connector failure
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
- 2026-05-20FDA-DeviceDJO, LLCClass IIDJO DONJOY ICEMAN CLASSIC CUBE recalled for connector failure
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
- 2026-05-20FDA-DeviceOn-X Life Technologies, Inc.Class IIOn-X mitral heart valves recalled for incomplete testing
Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.
- 2026-05-20FDA-DeviceWindstone Medical Packaging, Inc.Class IWindstone Custom Convenience Kit recalled for syringe disconnection risk
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.
- 2026-05-20FDA-DeviceOmnicell, Inc.Class IOmnicell i.v.Station labels recalled for mislabeling risk
Potential for mislabeled syringe produced by the i.v.STATION device.
- 2026-05-20FDA-FoodSugar Foods LLCClass IKroger Homestyle Cheese and Garlic Croutons recalled for Salmonella risk
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.
- 2026-05-20FDA-FoodOcinet, Inc.Class II...And Kimchi recalled for undeclared fish allergen
Undeclared allergen ingredient (fish)
- 2026-05-20FDA-FoodProspector Popcorn, LLCClass IIProspector Popcorn recalled for undeclared soy
Products contain undeclared soy, specifically soy lecithin.
- 2026-05-20FDA-FoodRaja Foods and Vegetables Inc.Class IISwad Mango Masala Candy recalled for undeclared Blue 1
Contains undeclared Blue 1
- 2026-05-20FDA-FoodRaja Foods and Vegetables Inc.Class IISwad Orange Flavored Masala Candy recalled for undeclared dye
Contains undeclared FD&C Yellow 6
- 2026-05-20FDA-FoodWE R NUTSClass IIUncle Giuseppe's Bridge Mix recalled for undeclared allergens
Contains undeclared allergens (cashews, milk, and soy).
- 2026-05-20FDA-FoodFerris Coffee and Nut Company, Inc.Class IIFrederik's by Meijer trail mix recalled for undeclared wheat, soy
Undeclared allergens (wheat and soy).
- 2026-05-20FDA-FoodFINESALER LLCClass IIAlain Milliat Orange Marmalade recalled for glass pieces
Product may contain foreign objects, specifically glass.
- 2026-05-20FDA-FoodDakota Honey CompanyClass IIDakota Honey Company Honey Flight recalled for metal and plastic contamination
Foreign object (stainless steel dust/flakes or shreds of plastic)