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. 989 recalls have been distributed to West Virginia in the last 12 months.
Showing 18281–18300 of 48,376 recalls
Recalled Item: Acrysof Recalled by Alcon Research LLC Due to Incorrect IOL diopter
The Issue: Incorrect IOL diopter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553)...
The Issue: This product has been confirmed to exhibit holes in the packaging, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta MONACO RTP Sytem Recalled by Elekta Inc Due to The Monaco RTP...
The Issue: The Monaco RTP Radiation Treatment Planning System may change the shape and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System - Product Usage: Intended for use Recalled by...
The Issue: There is potential for a white paper-type residue attached to the catheter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cefixime for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Subpotent Drug: low out of specification (OOS) test result observed in long...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KORE ORGANIC CBD Oil Watermelon 15mg* Recalled by Summitt Labs Due to...
The Issue: Chemical Contamination; product contains elevated levels of lead
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nizatidine Oral Solution Recalled by Amneal Pharmaceuticals of New York, LLC...
The Issue: CGMP Deviations: potential N-Nitrosodimethylamine (NDMA) amounts above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Finasteride Plus 1.25 mg Capsule Recalled by MasterPharm LLC Due to Cross...
The Issue: Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Recalled by B & B Pharmaceuticals, Inc. Due to Foreign Object...
The Issue: cGMP deviations: Presence of foreign material (Teflon)introduced at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD BBLTM Gram Crystal Violet 3.8L-- IVD Primary stain for Recalled by Becton...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBLTM Gram Stain Kit with Stabilized Iodine-- IVD For Recalled by Becton...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Recalled by...
The Issue: May exhibit increased levels of artifacts which could be difficult to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 C17/5 - ceramic for dental...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - Recalled by...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.