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 621640 of 56,506 recalls

Medical DeviceDecember 2, 2025· Microbiologics Inc

Recalled Item: LYFO DISK Recalled by Microbiologics Inc Due to Affected units may fail to...

The Issue: Affected units may fail to recover the target microorganism Campylobacter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2025· Zimmer, Inc.

Recalled Item: Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus...

The Issue: Affected implants may have undersized distal diameter along length of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2025· HANGZHOU BEVER MEDICAL DEVICES CO., LTD.

Recalled Item: BD Ready-to-Use Hydrophilic Catheter 14 Fr (4.7 mm) Straight Tip Recalled by...

The Issue: Labeling error, Incorrect expiration date

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2025· Baxter Healthcare Corporation

Recalled Item: SIGMA Spectrum Infusion Pump Recalled by Baxter Healthcare Corporation Due...

The Issue: Certain pumps have potentially been released from service with defective...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Clindamycin Phosphate USP Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due...

The Issue: Failed Impurities/Degradation: Out of Specification results for Total...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed Recalled by...

The Issue: Medline Industries has identified a potential hazard involving the hand...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: MEDLINE beds labeled as: Full Electric Low Basic Homecare Bed Recalled by...

The Issue: Medline Industries has identified a potential hazard involving the hand...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed Recalled by...

The Issue: Medline Industries has identified a potential hazard involving the hand...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed Recalled...

The Issue: Medline Industries has identified a potential hazard involving the hand...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed Recalled by...

The Issue: Medline Industries has identified a potential hazard involving the hand...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed Recalled by...

The Issue: Medline Industries has identified a potential hazard involving the hand...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2025· Medline Industries, LP

Recalled Item: Medline Kits containing B. Braun IV Administration Sets and Pump Recalled by...

The Issue: Medline kits contain B. Braun IV Administration Sets and Pump Administration...

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

Class II — Potential Health HazardOngoing