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. 1,655 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
1,655 in last 12 months

Showing 4604146060 of 48,376 recalls

DrugNovember 30, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Carisoprodol Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Labeling: Not elsewhere classified: On 12/12/11, DEA published a final rule...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 30, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets Recalled by West-ward...

The Issue: Presence of Foreign Substance: Reports of gray smudges identified as minute...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 29, 2012· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: CO2 Incubators (General Purpose Incubator) Recalled by Thermo Fisher...

The Issue: Incubators manufactured prior to mid 2009 have coated metal hinges that have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2012· Handicare Accessibility

Recalled Item: Handset component of the Handicare USA's Minivator Bath Bliss Reclining...

The Issue: Firm became aware that two handsets in the affected batches became...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2012· Philips Healthcare Inc.

Recalled Item: Mobile Diagnostic X-Ray System with Digital Panel Recalled by Philips...

The Issue: When the operator moves an image to another view then the electronic marker...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2012· DePuy Orthopaedics, Inc.

Recalled Item: Pinnacle Cancellous Screw Packaging: Product is housed within a polyurethane...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary recall of ten lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2012· Beckman Coulter Inc.

Recalled Item: Beckman Coulter AU5800 Clinical Chemistry Analyzer. An automated chemistry...

The Issue: Due to a software data storage limitation which only occurs under certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 28, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: Mindray DS USA Recalled by Mindray DS USA, Inc. d.b.a. Mindray North America...

The Issue: Mindray has identified a software anomaly that may where, in the presence of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Somatom CTs equipped with software syngo CT2010A Recalled by Siemens...

The Issue: Sporadic hang-up malfunctions concerning 3D reconstructions during activated...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2012· Radiometer America Inc

Recalled Item: TCM4 series Base Units Recalled by Radiometer America Inc Due to RADIOMETER...

The Issue: RADIOMETER became aware that the TCM4 series Base Unit does not comply with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: DBS MICROPLATE Recalled by Perkinelmer Due to Truncated V-Bottomed...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: Microplate Recalled by Perkinelmer Due to Truncated V-Bottomed Microplate...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: NEOBASE NON-DERIVATIZED MSMS KIT Product Number: 3040-001U. This tandem mass...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Axiom Artis zeego systems with software version VC14 Recalled by...

The Issue: In the course of the firm's product monitoring activities, a potential risk...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: NEOGRAM AMINO ACIDS AND ACYLCARNITINES TANDEM MASS SPECTROMETRY KIT Product...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Perkinelmer

Recalled Item: NEONATAL TOTAL GALACTOSE KIT Product Numbers: 3029-0010 Recalled by...

The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2012· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...

The Issue: GranuFlo Dry Acid Concentrate may show discoloration

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

Class III — Low RiskOngoing