Vehicles & Parts
HIGH
Recall database
All Product Recalls
Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
- Active recalls
- 4,434
- Current page
- 138
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Food & Beverages
HIGH
FDA FOOD
Lunds & Byerlys Monster Cookies Recalled Due to Undeclared Allergens
Lunds & Byerlys recalled 1,296 cookies on December 3, 2025, due to undeclared allergens including peanuts, eggs, and soy. The recall affects 108 cases of Monster Cookies sold in Minnesota. Consumers should not eat the product and seek a refund.
Lund Food Holdings
Undeclared allergens
Health & Personal Care
HIGH
FDA DEVICE
Medtronic Recalls Vanta Clinician Programmer Software Over Functionality Issues
Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure.
Medtronic Neuromodulation
Complaints received
Food & Beverages
HIGH
FDA FOOD
Bendon Recalls Paw Patrol and Other Gummy Candies Over Hazardous Additive
Bendon, Inc. recalled 39,171 units of various gummy candies on December 3, 2025. The recall stems from the use of an unapproved color additive, chlorophyllin copper complex. Affected products include Paw Patrol, Mickey Mouse, and SpongeBob Squarepants gummies.
Bendon Publishing
Unapproved color
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Recalls Balloon Catheters Over Inflation Issues
Boston Scientific
Boston Scientific
Health & Personal Care
HIGH
FDA DEVICE
CareFusion 303 Recalls Automated Dispensing Cabinets Over Software Issues
Due a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems.
CareFusion 303
Due a
Health & Personal Care
HIGH
FDA DEVICE
Philips Incisive CT Recalled Over Scan Incompletion Risk
Potential for incomplete scan due to unstable connection inside of floating sensor.
Philips Healthcare
Potential for
Food & Beverages
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Philips MR 7700 Systems Recalled Due to Stiffness Value Errors
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips North America Recalls MR Systems Over Stiffness Value Errors
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls Ingenia Elition S MR Systems Over Stiffness Errors
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips North America Recalls MR Imaging System Over Stiffness Errors
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips MRI System Recalled Due to Stiffness Value Errors
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips North America Recalls Ingenia 3.0T MR Systems Over High Hazard
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips North America Recalls MR Systems Over Stiffness Value Errors
Philips North America recalled three MR systems on December 3, 2025. The recall affects models with software versions R11.1 and R12.1 due to potential stiffness value errors. Healthcare providers and patients must stop using these devices immediately.
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips North America Issues Recall of MR Systems Due to High Hazard Risk
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls Ingenia Ambition S MR Systems Over Stiffness Errors
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips North America Recalls MR Systems Over Stiffness Value Errors
Philips North America recalled six MR systems on December 3, 2025. The recall affects devices with software versions R11.1 and R12.1 due to potential stiffness value errors. Healthcare providers must stop using the affected units immediately.
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalled Ingenia Ambition X MR Systems Over Stiffness Errors
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential
Health & Personal Care
HIGH
FDA DEVICE
Philips North America Recalls MR Systems Due to Stiffness Value Errors
The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Philips North America
The potential