Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,677 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
1,677 in last 12 months

Showing 4748147500 of 48,219 recalls

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 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· 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 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: 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: 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: 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: 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 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: 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: 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 1 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 15, 2012· Polymer Technology Systems, Inc.

Recalled Item: PTS Panels Creatinine test strips. PTS Panels Creatinine Test Strips...

The Issue: During a routine product investigation, a creatinine sample with a value...

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

Class II — Potential Health HazardOngoing