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. 2,372 recalls have been distributed to West Virginia in the last 12 months.
Showing 22921–22940 of 48,376 recalls
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Presence of Particulate Matter: Product complaints received of grey flecks,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nutty Choco Pop Recalled by Funky Chunky LLC Due to Nutty Choco Pop has in...
The Issue: Nutty Choco Pop has in incorrect label and does not declare that it contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Phoenix AP AST Indicator Bag Recalled by Becton Dickinson & Co. Due to...
The Issue: Panels inoculated using certain lots of the indicator solution are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The WinStation Retinal Imager Recalled by Merge Healthcare, Inc. Due to...
The Issue: Certain configurations of Merge Eye Station hardware may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix AST-s Indicator Recalled by Becton Dickinson & Co. Due to Panels...
The Issue: Panels inoculated using certain lots of the indicator solution are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 3000 Series Washer/Disinfector Model # 3052 Recalled by Steris...
The Issue: The software in the systems may not process the cycle originally intended....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO 5000 Series Washer/Disinfector Model # 5052 Recalled by Steris...
The Issue: The software in the systems may not process the cycle originally intended....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Centricity Universal Viewer Breast Imaging Centricity...
The Issue: When switching back & forth between multiple UV instances in the Windows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoaguChek XS PT Test Recalled by TERRIFIC CARE LLC Due to Potential for...
The Issue: Potential for abnormally high INR test results with the CoaguChek XS PT Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix AST Indicator Recalled by Becton Dickinson & Co. Due to Panels...
The Issue: Panels inoculated using certain lots of the indicator solution are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stingray" Guidewire Recalled by Boston Scientific Corporation Due to A batch...
The Issue: A batch of 185cm Stingray Guidewires are incorrectly labeled as 300cm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...
The Issue: A software update is being issued to correct multiple issues identified in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fungitell Kit Recalled by Associates of Cape Cod, Inc. Due to The kits may...
The Issue: The kits may contain the incorrect number of components or the kits may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Pleasure Pack (60 ct) Recalled by Reckitt Benckiser LLC Due to Five...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Cincinnati Sub-Zero...
The Issue: Evidence supports that when customers performed a fuse replacement as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Real Feel Recalled by Reckitt Benckiser LLC Due to Five batches of the...
The Issue: Five batches of the product have failed the specification of 1.0kPa for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Gastrointestinal Suture Anchor Set Recalled by Cook Inc. Due...
The Issue: There is a potential for difficulty in sliding down the retention mechanism...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix Lumbar Spinal Implant System: 22mm x 10mm x 7mm PLIF ASSY PC Recalled...
The Issue: This recall has been initiated due to a change in packaging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olmesartan Medoxomil and Hydrochlorothiazide Tablets Recalled by Teva...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.