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. 2,525 recalls have been distributed to West Virginia in the last 12 months.
Showing 8321–8340 of 48,376 recalls
Recalled Item: Impella 2.5 intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP intravascular micro axial blood pump Recalled by Abiomed, Inc....
The Issue: There is a potential risk for unintentional interaction of the Impella motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dry Eye Relief Lubricant Eye Drops Recalled by K.C. Pharmaceuticals, Inc Due...
The Issue: CGMP Deviations: good manufacturing deficiencies related to a lack of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Original Eye Drops Recalled by K.C. Pharmaceuticals, Inc Due to CGMP...
The Issue: CGMP Deviations: good manufacturing deficiencies related to a lack of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tranexamic Acid USP Tablets Recalled by AVKARE LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Randox RX Series Urea Enzymatic Kinetic Assay Ref. Numbers: (1) Recalled by...
The Issue: Carryover from the Direct LDL-cholesterol assay on the Rx instruments may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2 Recalled...
The Issue: Dura regeneration matrix may have out-of-specification endotoxin levels due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endometrin (progesterone) Vaginal Insert 100mg Recalled by Ferring...
The Issue: cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lysteda (tranexamic acid) USP Tablets Recalled by Amring Pharmaceuticals Inc...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Havasu Beetroot Powder Recalled by Supplement Manufacturing Partner, Inc....
The Issue: Contains undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 7700 Magnetic Resonance (MR) system Recalled by Philips North America Due...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: The system operator is able to bypass the SmokeDetector Interlock system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Magnetic Resonance (MR) system Recalled by Philips North...
The Issue: During installation of the SmokeDetector Interlock, a connecting cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20. X-ray Image guided Therapy System. Recalled by PHILIPS...
The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 and FD20. X-ray Imaging System. Recalled by PHILIPS MEDICAL...
The Issue: The bolts supporting the FlexMove Carriage may become loose and/or break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxylog 3000 Plus emergency and transport ventilator Recalled by Draeger...
The Issue: Draeger has become aware of instances where the device stopped working when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Amplatzer Steerable Delivery Sheath (ASDS) Recalled by Abbott Due to...
The Issue: There is an overall reported incidence rate of 0.77% related to observed or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.