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. 2,345 recalls have been distributed to West Virginia in the last 12 months.
Showing 32921–32940 of 48,376 recalls
Recalled Item: Organic Root Medley Recalled by CRF Frozen Foods, LLC Due to Potential...
The Issue: Organic Root Medley is recalled because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...
The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...
The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...
The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...
The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...
The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...
The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sclerosol Intrapleural Aerosol (sterile talc powder) Recalled by Lymol...
The Issue: Defective Delivery System: Defective stem valve causes leakage of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zoloft (sertraline HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: thick tablets exceeding specifications...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Walnut Delights 6 Pack Net Weight: 9 oz. PLU #69690 Recalled by Giant Eagle,...
The Issue: Giant Eagle discovered that the scale label fails to declare the milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pecan Tassie - 6 Pack PLU# 77997 Net Wt. 5 OZ. Sell By (dates up to) May 03...
The Issue: Giant Eagle discovered that the scale label fails to declare the milk...
Recommended Action: Do not consume. Return to store for a refund or discard.