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 22761–22780 of 48,376 recalls
Recalled Item: Lipid Panel test strips Recalled by Polymer Technology Systems, Inc. Due to...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHOL+HDL+GLU test strips Recalled by Polymer Technology Systems, Inc. Due to...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipid Panel test strips (as a component of smart bundles) Recalled by...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences(R) IntraClude(TM) Intra-Aortic Occlusion Device is a...
The Issue: Edwards Lifesciences has received a limited number of customer reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF) Recalled by KRS...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF) Recalled by KRS...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by LUPIN SOMERSET Due to...
The Issue: Failed Impurities/Degradation Specifications: Expansion of October 2018...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: infants* IBUPROFEN Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ezetimibe and Simvastatin Tablets 10mg/80 mg Recalled by Dr. Reddy's...
The Issue: Presence of Foreign Substance: Product complaint of black speckles observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Infant Mask Recalled by...
The Issue: A repair was made to an adapter mold resulting in parts being produced with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit With Neonatal Mask Recalled by...
The Issue: A repair was made to an adapter mold resulting in parts being produced with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Vent Infant T-Piece Resuscitation Circuit Recalled by Westmed, Inc. Due...
The Issue: A repair was made to an adapter mold resulting in parts being produced with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proximal Humerus Plate Recalled by Miami Device Solutions, LLC. Due to Right...
The Issue: Right Proximal Humerus Plates. Product component parts MDS130108R, may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm FDR Go PLUS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...
The Issue: FUJIFILM Medical Systems U.S.A., Inc., Modality Systems became aware of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Urinary Drainage bag Recalled by Teleflex Medical Due to The device...
The Issue: The device labels are not UDI compliant. The missing UDI compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH CARE Premium Drain bag Recalled by Teleflex Medical Due to The device...
The Issue: The device labels are not UDI compliant. The missing UDI compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is...
The Issue: Normal operation of the device is to power up the device in the morning,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Burr Recalled by Arthrex, Inc. Due to Devices may generate excessive...
The Issue: Devices may generate excessive heat during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.