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. 2,393 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,393 in last 12 months

Showing 2154121560 of 27,884 recalls

Medical DeviceJune 29, 2015· Merit Medical Systems, Inc.

Recalled Item: ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are...

The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Baxter Healthcare Corp.

Recalled Item: Baxter HomeChoice and HomeChoice Pro APD systems Recalled by Baxter...

The Issue: Loud operating sounds, which was unacceptable to the end users when the...

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

Class III — Low RiskOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q systems Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics MacConkey Agar with CiPRP Recalled by Hardy Diagnostics...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Agar with Vancomycin container type: 15x100mm...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam Gamma Camera Recalled by Siemens Medical Solutions USA, Inc. Due to...

The Issue: Potential failure mode related to the radial brake, where the detector was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics MDR Acinetobacter container type: 15x100mm monoplate...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Broth with Vancomycin container type: 13x100mm tube...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Alere Scarborough, Inc. dba Binax, Inc.

Recalled Item: Alere i flu Recalled by Alere Scarborough, Inc. dba Binax, Inc. Due to Risk...

The Issue: Risk of false negative results due to microbial growth in the Sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics VRE Broth Recalled by Hardy Diagnostics Due to Hardy...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Agar with VGA container type: 15x100mm monoplate...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BHI with CIPRO Recalled by Hardy Diagnostics Due to Hardy...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON S 1000 Recalled by Siemens Medical Solutions USA, Inc. Due to...

The Issue: Potential measurement error on ACUSON S Family ultrasound system when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON S2000 and ACUSON S3000 ultrasound systems with the Virtual Recalled...

The Issue: Potential measurement error on ACUSON S Family ultrasound system. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical P-440 Portable Ceiling Lift Recalled by ErgoSafe Products, LLC...

The Issue: There is a potential the sling loops may not stay attached to the carry bar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· Zimmer Surgical Inc

Recalled Item: 18inch Dual Port/Single Bladder Disposable Tourniquet Cuff Recalled by...

The Issue: The inside of the folded Instructions For Use (IFU) pamphlet was missing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· EKOS Corporation

Recalled Item: The EKOS EkoSonic Control Unit is intended exclusively for use Recalled by...

The Issue: The Connector Interface Cable (CIC) was not recognized by the EkoSonic PT-3B...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical P-600 Portable Ceiling Lift Recalled by ErgoSafe Products, LLC...

The Issue: There is a potential the sling loops may not stay attached to the carry bar...

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

Class II — Potential Health HazardOngoing