Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 3,068 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,068 in last 12 months

Showing 25612580 of 30,923 recalls

Medical DeviceDecember 18, 2024· Braemar Manufacturing, LLC

Recalled Item: Monitoring Service Application (MSA). Software to process Recalled by...

The Issue: Not all Electrocardiogram (ECG) events received July 2022-July 2024 were not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 16, 2024· Augustine Temperature Management, LLC

Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...

The Issue: There is over-molding that stabilizes the connection between the cable and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Augustine Temperature Management, LLC

Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...

The Issue: There is over-molding that stabilizes the connection between the cable and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Augustine Temperature Management, LLC

Recalled Item: Hot Dog PATIENT WARMING Recalled by Augustine Temperature Management, LLC...

The Issue: There is over-molding that stabilizes the connection between the cable and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Recalled...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· Integra LifeSciences Corp.

Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...

The Issue: Potential for certain SKUs and lot numbers were distributed with the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) MTO Recalled by MEDLINE...

The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 16, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) FDS Recalled by MEDLINE...

The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 16, 2024· Olympus Corporation of the Americas

Recalled Item: LithoCrushV Single Use Mechanical Lithotriptor V. Model Number:...

The Issue: Potential for distal tip tearing of the Mechanical Lithotriptor V.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2024· Alphatec Spine, Inc.

Recalled Item: Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1)...

The Issue: Complaints have been received regarding post-operative implant collapse.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Wolf-Pak Product Name: Premium Dressing Change Kit with Recalled...

The Issue: Potential for hole in package compromising sterility of the medical kit.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: IMed Products Product Name: Dressing Change Kit with Recalled by...

The Issue: Potential for hole in package compromising sterility of the medical kit.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Recalled...

The Issue: Potential for hole in package compromising sterility of the medical kit.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Transparent...

The Issue: Potential for hole in package compromising sterility of the medical kit.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Trinity Sterile, Inc.

Recalled Item: Brand Name: Tacy Medical Recalled by Trinity Sterile, Inc. Due to Potential...

The Issue: Potential for hole in package compromising sterility of the medical kit.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2024· Hologic, Inc.

Recalled Item: Panther Fusion GBS Assay Kit containing Panther Fusion Recalled by Hologic,...

The Issue: Potential weak pouch seal on Panther Fusion GBS assay cartridge, causing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2024· LivaNova USA, Inc.

Recalled Item: SenTiva Recalled by LivaNova USA, Inc. Due to Vagus nerve stimulator...

The Issue: Vagus nerve stimulator generators may stop delivering stimulation due to an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2024· LivaNova USA, Inc.

Recalled Item: SenTiva Recalled by LivaNova USA, Inc. Due to Vagus nerve stimulator...

The Issue: Vagus nerve stimulator generators may stop delivering stimulation due to an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2024· Medtronic Perfusion Systems

Recalled Item: DLP Pediatric One-Piece Arterial Cannulae Recalled by Medtronic Perfusion...

The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing