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 1980119820 of 30,923 recalls

Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· King Systems Corp. dba Ambu, Inc.

Recalled Item: UNIVERSAL FLEX2 BREATHING CIRCUIT Recalled by King Systems Corp. dba Ambu,...

The Issue: Potential for leak test failures.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11.5MM Product Number:...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing