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. 2,881 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,881 in last 12 months

Showing 1966119680 of 30,923 recalls

Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Knee/Shldr Recalled by Breg Inc Due to They may not have been...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Shldr XL Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing M/U XL Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Recalled by Breg Inc Due to They may not have been sealed prior to...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Back Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Shldr Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Rect L Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: If Hip Recalled by Breg Inc Due to They may not have been sealed prior to...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Newport Medical Instruments Inc

Recalled Item: Newport Medical HT70 and HT70- Plus Ventilators Recalled by Newport Medical...

The Issue: Medtronic is issuing a voluntary field corrective action for all its...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing