Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,266 recalls have been distributed to West Virginia in the last 12 months.
Showing 47641–47660 of 48,376 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Big Burst Kiwi Strawberry Drink in a 16 oz PET plastic bottle with a sports...
The Issue: There is a possibility that a part of the nozzle cap of the bottle can...
Recommended Action: Do not consume. Return to store for a refund or discard.