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 2478124800 of 27,884 recalls

Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster Recalled by Carl Zeiss Meditec, Inc. Due to The user...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Alere San Diego, Inc.

Recalled Item: Product Brand Name(s): Alere Cholestech LDX¿ Lipid Profile"GLU Test Cassette...

The Issue: Alere initiated a recall of Cholestech LDX Lipid Profile-GLU test cassettes,...

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

Class III — Low RiskOngoing
Medical DeviceOctober 23, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable Recalled by...

The Issue: It was reported that the siderail may appear latched when it is not, due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster 500 Recalled by Carl Zeiss Meditec, Inc. Due to The...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ Extra Support Guidewire Recalled by Medtronic Vascular Due to...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Urologix, Inc.

Recalled Item: Prostiva RF Therapy Hand Piece Kit Recalled by Urologix, Inc. Due to A Hand...

The Issue: A Hand Piece high deployment force exceeded the maximum specification.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ProVia¿ CROSSING GUIDEWIRE Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive has identified that the metalized coating on the IS3000 HD lamp...

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

Class III — Low RiskOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: COUGAR¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Vital Images, Inc.

Recalled Item: VitreaCore¿ software. Versions subject to the limitation: 6.0 Recalled by...

The Issue: Vital Images, Inc. has found an issue in VitreaCore software though internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: THUNDER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Applied Medical Resources Corp

Recalled Item: Applied Medical's Inzii¿ 12/15mm Retrieval System. Applieds Inzii Tissue...

The Issue: Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ Recalled by...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 18, 2013· Intra Pump Infusion Systems

Recalled Item: CRN Crono Syringe CRN20 with 19G x 1 "Steel Needle" Recalled by Intra Pump...

The Issue: Product has the potential to have a clear debris on the tip of the needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2013· Steris Corporation

Recalled Item: AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile...

The Issue: The firm discovered that unlatching can occur when overloaded transfer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2013· Advanced Sterilization Products

Recalled Item: Sterrad 100NX Recalled by Advanced Sterilization Products Due to Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the Sterrad 100NX...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Spacelabs Healthcare, Llc

Recalled Item: Spacelabs Healthcare qube Compact Patient Monitor Recalled by Spacelabs...

The Issue: Spacelabs Healthcare qube Compact Patient Monitor, Model 91390, may fail to...

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

Class II — Potential Health HazardOngoing