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. 2,356 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,356 in last 12 months

Showing 2708127100 of 27,884 recalls

Medical DeviceJuly 10, 2012· AGFA Corp.

Recalled Item: IMPAX CV Reporting The Results Management (RM)/IMPAX CV reporting component...

The Issue: When users selected "Left stenosis" in the "Graft Duplex Conclusion" section...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2012· GE Healthcare, LLC

Recalled Item: Optima XR200amx. Mobile general purpose radiographic imaging of the human...

The Issue: Software issue: a violation of 21 CFR 1020.31(a). After an image is taken,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Iris Diagnostics

Recalled Item: IRISpec" CA/CB two-part urine chemistry control twin set Recalled by Iris...

The Issue: The firm recalled after it received complaints of IRISpec CA/CB two part...

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

Class III — Low RiskOngoing
Medical DeviceJuly 9, 2012· Sentec AG

Recalled Item: SenTec Recalled by Sentec AG Due to SenTec is recalling a number of V-Sign"2...

The Issue: SenTec is recalling a number of V-Sign"2 Sensors due to a problem regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Beekley Corporation

Recalled Item: Beekley O-Spots Floral Skin Markers -Order Number: 752 Product Usage:...

The Issue: Digital Skin Mammography Marker separating from the backing of the spot material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Beekley Corporation

Recalled Item: Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: Recalled...

The Issue: Digital Skin Mammography Marker separating from the backing of the spot material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Beekley Corporation

Recalled Item: Beekley A-Spots Floral Skin Markers -Order Number: 751 Product Usage:...

The Issue: Digital Skin Mammography Marker separating from the backing of the spot material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2012· Beekley Corporation

Recalled Item: Beekley S-Spots Floral Skin Markers -Order Number: 750 Product Usage:...

The Issue: Digital Skin Mammography Marker separating from the backing of the spot material

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2012· FMS, Finapres Medical Systems BV

Recalled Item: Finapres Medical Systems Portapres with NiMh battery pack Product Usage:...

The Issue: Battery may become hot and leak

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2012· Baxter Healthcare Renal Div

Recalled Item: Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic...

The Issue: Baxter discovered that a Baxter technical service representative was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2012· Beckman Coulter Inc.

Recalled Item: Unicel Closed Tube Aliquotter (UCTA) for UniCel DxC 660i Recalled by Beckman...

The Issue: The recall was initiated because Beckman Coulter has confirmed that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Radiometer America Inc

Recalled Item: The ABL software version 6.12 for the ABL800 analyzer. The Recalled by...

The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Radiometer America Inc

Recalled Item: ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer Recalled by...

The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Kimberly-Clark Corporation

Recalled Item: ULTRA Fabric Reinforced surgical Gown X-Large Sterile The product is...

The Issue: Package seam of some units may not remain properly sealed to ensure the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Stryker Spine

Recalled Item: Aviator Drill Bit (10 mm Recalled by Stryker Spine Due to Aviator drill bits...

The Issue: Aviator drill bits are 10 mm longer than the Hybrid drill bits and are not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Kimberly-Clark Corporation

Recalled Item: MicroCool Breathable Gown with Towels Recalled by Kimberly-Clark Corporation...

The Issue: Package seam of some units may not remain properly sealed to ensure the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2012· Radiometer America Inc

Recalled Item: The ABL software version 6.12 for the ABL800 and ABL700 Recalled by...

The Issue: A customer has reported an error on an ABL8xx configured to a Hospital...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Hoffman LRF Telescopic Strut Short Stryker Stryker Trauma AG CH-2545...

The Issue: Three complaints have been filed where the Hoffman LRF Telescopic Struts...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2012· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor Recalled by Smith &...

The Issue: Distal part of the anchor may break on insertion into bone during surgery

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2012· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with three #2 sutures (white...

The Issue: Distal part of the anchor may break on insertion into bone during surgery

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

Class II — Potential Health HazardOngoing