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. 2,380 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,380 in last 12 months

Showing 2302123040 of 27,884 recalls

Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Veta Peritoneal Catheter Kit Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT Peritoneal Drainage System Recalled by Pfm Medical Inc Due to PFM...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: 6F x 60 cm Dual Lumen CT PICC Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: ASEPT Pleural Drainage System Recalled by Pfm Medical Inc Due to PFM Medical...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Micro Introducer Kit Recalled by Pfm Medical Inc Due to PFM Medical is...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Radiometer America Inc

Recalled Item: HemoCue¿ Glucose 201 Microcuvettes Recalled by Radiometer America Inc Due to...

The Issue: Batches of HemoCue Glucose 201 Microcuvettes show discoloration and provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Pfm Medical Inc

Recalled Item: Thoracentesis & Paracentesis Procedure Tray Recalled by Pfm Medical Inc Due...

The Issue: PFM Medical is recalling catheters and other medical devices because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-EBV-VCA IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2014· Diamedix Corporation

Recalled Item: Diamedix Is-EBV-EA-D IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by...

The Issue: A gel-like substance was found in kit component, sample diluent , that could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2014· Biosense Webster, Inc.

Recalled Item: ThermoCool SmartTouch Navigation Catheters Recalled by Biosense Webster,...

The Issue: The recall was initiated because Biosense Webster is providing additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide...

The Issue: Cardiohelp- i System may have a software issue that can potentially result...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Ethicon, Inc.

Recalled Item: Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet...

The Issue: Ethicon is unable to ensure that PERMA-HAND silk suture (siliconized black...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Rapid Neg Urine Combo Panel Type 1 Recalled by Siemens Healthcare...

The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Rapid Neg BP Combo Panel Type 3 Recalled by Siemens Healthcare Diagnostics,...

The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Biomerieux

Recalled Item: Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility...

The Issue: The products have a wrong expiration date on their labeling, 5 years instead...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2014· Materialise USA LLC

Recalled Item: Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Recalled...

The Issue: The box of guides for a specific case arrived intact but contained two (2)...

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

Class II — Potential Health HazardOngoing