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. 2,393 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,393 in last 12 months

Showing 2238122400 of 27,884 recalls

Medical DeviceFebruary 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008 Series Hemodialysis Machines: 2008T with the following product code...

The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008 Series Hemodialysis Machines: 2008K2 with the following product code...

The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008 Series Hemodialysis Machines: 2008K with the following product code...

The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Pega Medical Inc.

Recalled Item: GAP Nail 4.8mm (diameter size) of the GAP ENDO-EXO MEDULLARY Recalled by...

The Issue: Failures of the 4.8mm of the GAP Endo-Exo Medullary System have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· ArthroCare Medical Corporation

Recalled Item: Coblator II System Recalled by ArthroCare Medical Corporation Due to The...

The Issue: The recalling firm was notified by the contract manufacturer that they had...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2015· Steris Corporation

Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers Recalled by Steris Corporation Due...

The Issue: STERIS has identified that the control board software in select AMSCO 400...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2015· Steris Corporation

Recalled Item: Caviwave Pro Ultrasonic Cleaning System Recalled by Steris Corporation Due...

The Issue: Should the Caviwave Pro Ultrasonic Cleaning System experience a temporary...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2015· CHG Hospital Beds Inc

Recalled Item: The Spirit TM Select bed is a Med-Surg bed intended Recalled by CHG Hospital...

The Issue: It was identified that in some situations the bed exit alarm may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· US Endoscopy Group Inc

Recalled Item: Velocity" Biopsy Valve Recalled by US Endoscopy Group Inc Due to The company...

The Issue: The company has received reports of structural non conformance at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· Synthes, Inc.

Recalled Item: Thumb Screw for the Synthes Recon Locking Aiming Arm for Recalled by...

The Issue: For certain lots, the incorrect raw material of annealed 17-4PH Stainless...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· King Systems Corp.

Recalled Item: Double Swivel Connector with Suction Port Connector Recalled by King Systems...

The Issue: Product is mislabeled as Double Swivel Connector with Suction Port and is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2015· Transonic Systems Inc

Recalled Item: Transonic Hemodialysis Monitor Recalled by Transonic Systems Inc Due to...

The Issue: Customer unable to obtain measurements due to the device seeing no flow or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2015· Medela Inc. EF Division

Recalled Item: - NTL-30 30ml Nutrio Enteral Feeding Syringe (sterile) - NTL-60 Recalled by...

The Issue: The firm is recalling sterile enteral feeding syringes due to determining...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2015· Exactech, Inc.

Recalled Item: Equinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic...

The Issue: Incorrectly packaged. Outer and inner labeling may incorrectly identify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Ameda, Inc.

Recalled Item: Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115)...

The Issue: Devices were not sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Dako North America Inc.

Recalled Item: Autostainer Link 48 (AS480) Recalled by Dako North America Inc. Due to A...

The Issue: A false negative result affecting the diagnosis may occur. A defect in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon...

The Issue: Potential for weld disassociation of the cross pin, which could lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Ameda, Inc.

Recalled Item: Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging Recalled...

The Issue: Devices were not sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Sybron Dental Specialties

Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...

The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· DePuy Orthopaedics, Inc.

Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...

The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....

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

Class II — Potential Health HazardOngoing