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. 2,450 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,450 in last 12 months

Showing 1808118100 of 27,884 recalls

Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Merit Medical Systems, Inc.

Recalled Item: 1 mL Medallion¿ Syringe. Catalog Numbers: 701989001 Recalled by Merit...

The Issue: Merit Medical Systems announces a voluntary field action for the 1mL...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Sysmex America Inc

Recalled Item: Sysmex Recalled by Sysmex America Inc Due to Reported customer complaints of...

The Issue: Reported customer complaints of automated hematology analyzers catching fire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2017· Toshiba American Medical Systems

Recalled Item: Toshiba Medical Radrex - i Digital Radiography X-ray system Radrex-i...

The Issue: It was discovered during a procedure that when the operator made an exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Cook Medical Incorporated

Recalled Item: Zenith Alpha Thoracic Endovascular Graft The Zenith Alpha" Thoracic...

The Issue: There have been five reports of graft thrombosis/occlusion during global...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2017· Tosoh Bioscience Inc

Recalled Item: AIA-360 Analyzer is capable of performing two methods of immunoassay:...

The Issue: The firm has become aware of a potential issue with the AIA-360 analyzer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· ReFlow Medical

Recalled Item: Wingman 35 Crossing Catheter Recalled by Medical Due to Medical is recalling...

The Issue: Medical is recalling the Wingman 35 Crossing Catheter because it may be...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: Allura Xper Release 8.2 (Laird chiller is always installed) Recalled by...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: UNIQ: UNIQ FD10 722026 Recalled by Philips Electronics North America...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX Recalled by Zimmer...

The Issue: pegs shearing post-operatively

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2017· Philips Electronics North America Corporation

Recalled Item: The following systems are only affected if a Laird chiller Recalled by...

The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2017· Roche Diagnostics Corporation

Recalled Item: Sample probes associated with: cobas 6000 Series System Recalled by Roche...

The Issue: Due to a design change in 2015, corrosion on the sample probe electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue (R)...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology A PICC permits venous access Recalled...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit The Arrow¿...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Arrow(R) Access Kit for use with 4 Fr. Peripherally Inserted Recalled by...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath Recalled...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous...

The Issue: Arrow International initiated the recall due to reports of safety cover...

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

Class II — Potential Health HazardOngoing