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 2722127240 of 27,884 recalls

Medical DeviceJune 4, 2012· Leica Microsystems, Inc.

Recalled Item: Leica M525 F50 Surgical Microscope Recalled by Leica Microsystems, Inc. Due...

The Issue: Leica Microsystems evaluated data showing that a malfunction resulting in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2012· Aesculap, Inc.

Recalled Item: Aesculap(R) - Miethke Shunt System Recalled by Aesculap, Inc. Due to The...

The Issue: The deflector may not move freely on the ventricular catheter. The deflector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· I-Flow LLC

Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...

The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· I-Flow LLC

Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...

The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-5000 Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Sysmex America, Inc.

Recalled Item: Sysmex XE-2100C Automated Hematology System Recalled by Sysmex America, Inc....

The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T4-Hytrel Zipper Toga Product Usage - The togas are intended Recalled by...

The Issue: The clear tape, that is intended to aid in the prevention of patients...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Advanced Sterilization Products

Recalled Item: CIDEX OPA Recalled by Advanced Sterilization Products Due to The recall was...

The Issue: The recall was initiated because Advanced Sterilization Products has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick...

The Issue: Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips...

The Issue: Firm officials reported to CIN-DO that their Electrosurgical Monopolar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips Recalled by PSC...

The Issue: Firm officials reported to CIN-DO that the outer carton label of this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· PSC Industries Inc

Recalled Item: Bayonet Forceps 8.25 (209.6 mm) 0.5mm Tips Recalled by PSC Industries Inc...

The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2012· Stryker Instruments Div. of Stryker Corporation

Recalled Item: T5 Hytrel Zipper Toga. Product Usage: The togas are intended Recalled by...

The Issue: The clear tape, that is intended to aid in the prevention of patients fluids...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2012· Synthes (USA) Products LLC

Recalled Item: Universal Spinal System Lamina Hooks Synthes Medium TI Lamina Hook Recalled...

The Issue: USS Lamina Hooks, Medium, Right are being recalled because the hooks are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2012· SALTER LABS

Recalled Item: Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7...

The Issue: A complaint was received, and later verified, that product labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2012· Abbott Laboratories

Recalled Item: ARCHITECT CA 19-9XR Reagent Kit Recalled by Abbott Laboratories Due to The...

The Issue: The six ARCHITECT CA 19-9XR reagent lots are demonstrating a shift up in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2012· Alphatec Spine, Inc.

Recalled Item: TRESTLE LUXE¿ Anterior Cervical Plating System Recalled by Alphatec Spine,...

The Issue: On May 9th 2012 Alphatec Spine received a complaint which reported that the...

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

Class II — Potential Health HazardOngoing