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. 2,266 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,266 in last 12 months

Showing 4628146300 of 48,376 recalls

Medical DeviceOctober 23, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: The Siemens Symbia S series is intended to aid in detecting Recalled by...

The Issue: There is a potential for the linear bearing car to fail allowing the ball...

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

Class II — Potential Health HazardOngoing
DrugOctober 23, 2012· Estee Lauder Inc

Recalled Item: ESTEE LAUDER DayWear Sheer Tint Release Recalled by Estee Lauder Inc Due to...

The Issue: Failed Stability Specifications: The active sunscreen ingredient, avobenzone...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 22, 2012· Hospira Inc.

Recalled Item: HEXTEND 6% Hetastarch in Lactated Electrolyte Injection Recalled by Hospira...

The Issue: Lack of Assurance of Sterility: There is the potential for the solution to...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2012· Zi Xiu Tang Success, LLC

Recalled Item: Ultimate Formula Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 22, 2012· Zi Xiu Tang Success, LLC

Recalled Item: Classic Zi Xiu Tang Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Calibration Verification Recalled by Alere San Diego,...

The Issue: Out of range (increased) HDL Cholesterol results.

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

Class III — Low RiskOngoing
Medical DeviceOctober 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Multianalyte Control Recalled by Alere San Diego, Inc....

The Issue: Out of range (increased) HDL Cholesterol results.

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

Class III — Low RiskOngoing
Medical DeviceOctober 22, 2012· Becton Dickinson & Co.

Recalled Item: BD BBL Taxo XV Factor Strips Recalled by Becton Dickinson & Co. Due to In...

The Issue: In vitro diagnostic test kit was not manufactured according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· TITAN SPINE, LLC

Recalled Item: Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard...

The Issue: Titan Spine LLC, is conducting a recall on the Endoskeleton TA VBR products....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· Innovative Magnetic Resonance Imaging Systems Inc.

Recalled Item: IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00)...

The Issue: IMRIS Inc. initiated a recall of their OR Tables ORT100 and ORT200. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· American Medical Systems, Inc.

Recalled Item: AMS AdVance" Male Sling System 720088-01 AMS AdVance" Male Sling Recalled by...

The Issue: American Medical Systems¿ (AMS) is issuing a voluntary recall on a number of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· Trivascular, Inc

Recalled Item: TriVascular brand Fill Polymer Kit Recalled by Trivascular, Inc Due to...

The Issue: Selected lots of the Fill Polymer Kit (European Model Number: TVFP14- B) in...

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

Class II — Potential Health HazardOngoing
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Zenchent (norethindrone and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Zovia (ethynodiol diacetate and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Necon 1/35-28 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Lutera (levonorgestrel and ethinyl estradiol) Tablets USP Recalled by Watson...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2012· Watson Laboratories Inc

Recalled Item: Necon 10/11 (norethindrone and ethinyl estradiol) Tablets USP Recalled by...

The Issue: Cross Contamination With Other Products: The firm recalled Zovia, Lutera,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 18, 2012· OrthoPediatrics Corp

Recalled Item: 4.5mm PLEO Osteotomy Guide. OrthoPediatrics Corp. markets a pediatric...

The Issue: Complaint received from sales representative that the drill guide tubes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2012· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Sliced CT Scanner System Recalled by Philips And Neusoft...

The Issue: The four screws that secure the patient table top to the carrier pulled out...

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

Class II — Potential Health HazardOngoing
FoodOctober 18, 2012· Gilster-Mary Lee Corp.

Recalled Item: Gilster-Mary Lee Corporation Recalled by Gilster-Mary Lee Corp. Due to...

The Issue: The Better Valu Fruit Whirls contain undeclared almond butter.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund