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. 2,649 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,649 in last 12 months

Showing 5572155740 of 56,506 recalls

Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 3 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 9 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 5 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 10 Packaging: The product was packaged within Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 6 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 7 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 4 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: LUSTER HIP SZ 8 Packaging: The product was packaged within Recalled by DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· DePuy Orthopaedics, Inc.

Recalled Item: ULTIMA*LX STM Recalled by DePuy Orthopaedics, Inc. Due to DePuy...

The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· Boston Scientific Corporation

Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 13mm UPN Outer Box:...

The Issue: Difficulty in extending snare loop from the catheter

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· Boston Scientific Corporation

Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 11mm UPN Outer Box...

The Issue: Difficulty in extending snare loop from the catheter

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2012· Boston Scientific Corporation

Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 27mm UPN Outer Box:...

The Issue: Difficulty in extending snare loop from the catheter

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

Class II — Potential Health HazardOngoing