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. 3,047 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,047 in last 12 months

Showing 52415260 of 30,923 recalls

Medical DeviceDecember 6, 2023· Accure Acne, Inc

Recalled Item: Accure Laser System Recalled by Accure Acne, Inc Due to Laser system's spot...

The Issue: Laser system's spot tracking system may become misaligned resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Flo-Thru Intraluminal Shunt Recalled by Baxter Healthcare Corporation...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Floseal Hemostatic Matrix Fast Prep Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Vascu-Guard Peripheral Vascular Patch (US) Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter FloSeal Hemostatic Matrix NL Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Flo-Rester Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: PERI-GUARD SUPPLE Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Coseal Premix Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Vascu-Guard Peripheral Vascular Patch (GLOBAL) Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Preveleak Surgical Sealant Recalled by Baxter Healthcare Corporation...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Ostene Hemostasis Material Recalled by Baxter Healthcare Corporation...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Vascular Probe Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter FloSeal Hemostatic Matrix RECOTHROM Recalled by Baxter Healthcare...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Baxter Healthcare Corporation

Recalled Item: Peri-Guard Repair Patch Recalled by Baxter Healthcare Corporation Due to...

The Issue: Cardiovascular Surgery marketing brochure (US-AS46-220001) that was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2023· Abiomed, Inc.

Recalled Item: Impella Connect Recalled by Abiomed, Inc. Due to The following features have...

The Issue: The following features have been disabled from the web-based portal because...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table version Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2023· Oakworks Inc

Recalled Item: Ultrasound EA (Ergonomic Advantage) table versions Recalled by Oakworks Inc...

The Issue: Backrest platform stress fracture - the table is not operational in an...

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

Class II — Potential Health HazardOngoing