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. 2,521 recalls have been distributed to West Virginia in the last 12 months.
Showing 9541–9560 of 48,376 recalls
Recalled Item: Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobazam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobazam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP...
The Issue: CGMP Deviations: Potential risk of Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SafeLight Fiber Optic Cable: Clear Recalled by Stryker Corporation Due to...
The Issue: Fiber optic cables assembled with not enough epoxy on the proximal end,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CirClamp with 1.3cm Bell & Insert Reprocessed Recalled by MEDLINE...
The Issue: The CirClamp subassembly found in the kit was the incorrect size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for Recalled...
The Issue: Not programmed in accordance with specification. The programming affects the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium Recalled by B. Braun Medical Inc Due to Subpotent Drug: low...
The Issue: Subpotent Drug: low Anti-Factor IIa potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Ophthalmic Solution 0.15% Recalled by Apotex Corp. Due...
The Issue: Lack of sterility assurance: Cracks have developed in some of the units caps...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DG Health brand Sugar Free Daily Fiber in 10 oz. Recalled by Dollar General...
The Issue: Product is missing warning declaration that it contains phenylalanine.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Titan Pump Assembly Recalled by Coloplast Manufacturing US, LLC Due to A...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan NB Scrotal Zero Ang 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Scrot Zero 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Scro Zero Ang 22cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Scro Zero Ang 20cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Step Bladeless Trocars Recalled by Covidien, LP Due to Medtronic was made...
The Issue: Medtronic was made aware of a supplier calibration issue during the contract...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan 0-Deg Scrotal 20 Cm Recalled by Coloplast Manufacturing US, LLC Due to XXX
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Scro Zero Ang 16cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch NB Scrot Zero 16cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shanghai United Imaging Healthcare Co. Recalled by Shanghai United Imaging...
The Issue: Due to a software issue where the process of patient scanning, the scatter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Touch Infr Zero Ang 18cm Recalled by Coloplast Manufacturing US, LLC...
The Issue: A decrease in wall thickness has the potential for a premature pump failure,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.