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. 2,367 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,367 in last 12 months

Showing 2566125680 of 27,884 recalls

Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Unitized BactiSeal...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Siphonguard Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with SiphonGuard Device...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve only with SiphonGuard...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve with Catheter and Recalled by...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2013· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas Programmable Valve In Line Valve Only Product Code: Recalled...

The Issue: Codman Certas Programmable Valves used for hydrocephalus may not operate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Sysmex America Inc

Recalled Item: pocH-100i Recalled by Sysmex America Inc Due to The data printed on the...

The Issue: The data printed on the thermal printer may omit a digit or decimal point in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Four Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp....

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Two Lead Arthroscopic Irrigation Set Recalled by Baxter Healthcare Corp. Due...

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Baxter Healthcare Corp.

Recalled Item: Four Lead TUR irrigation Set Recalled by Baxter Healthcare Corp. Due to A...

The Issue: A firm's internal investigation led to the discovery of pinholes in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Biomet, Inc.

Recalled Item: Superior Approach Resection Guide Assembly. Indicated for primary Recalled...

The Issue: Biomet has initiated this action following an investigation which identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· Maytex Corp

Recalled Item: Comfort brand Ear-Loop Face Mask Recalled by Maytex Corp Due to Recent Lab...

The Issue: Recent Lab testing conducted in March 2013 indicates that the product does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2013· AGFA Corp.

Recalled Item: AGFA Digital Radiography X-Ray System DX-D 100 Agfa's DX-D 100 Recalled by...

The Issue: Customers could potentially experience intermittent, unintended and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Edwards Lifesciences, LLC

Recalled Item: QuickDraw Venous Cannula with Insertion Kit. ThruPort Systmes. Models QD22...

The Issue: Edwards is recalling the QuickDraw Venous Cannula due to complaints of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Optovue, Inc.

Recalled Item: Optovue iVue with Normative Database (NDB) with Software Version 3.0...

The Issue: Colors from the NDB comparison for Ganglion Cell Complex thickness in the...

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

Class III — Low RiskOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 100 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur iPTH Calibrator 2 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· GE Healthcare, LLC

Recalled Item: Canister: CO2 canister with GE part numbers 1407-3200-000 Recalled by GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH Calibrator 6 pk Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ iPTH ReadyPack Assay 500 Tests Recalled by Siemens Healthcare...

The Issue: iPTH Assay- reagent and calibrator lots may have demonstrated higher than...

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

Class II — Potential Health HazardOngoing