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. 2,356 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,356 in last 12 months

Showing 2728127300 of 27,884 recalls

Medical DeviceMay 21, 2012· Philips Healthcare Inc.

Recalled Item: Philips Multi Diagnost Eleva II with swivel cable Product Codes Recalled by...

The Issue: MultiDiagnost Eleva X--Ray system may have damage to System Cables from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to software...

The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2012· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Software For use in the in-vitro quantitative...

The Issue: software automatically switches the lot when a vancomycin (VANC) or valproic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: GoBed+ . Model FL20E Beds are intended for medical purposes Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Go Bed II+ Model FL 28 Ex Beds are intended Recalled by Stryker Medical...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker Rose Bed Model (FL14E) Beds are intended for medical Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker MA204 Bed Model (FL25E) Beds are intended for medical Recalled by...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 17, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Go Bed II+ Model FL28C Beds are intended for medical Recalled by Stryker...

The Issue: An adverse trend of scale and bed exit service reports/complaints were...

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: LUSTER HIP SZ 2 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· 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
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· 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 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· 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: 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