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 8581–8600 of 48,376 recalls
Recalled Item: Revize-X Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend MP Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend 4.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PriMatrix Meshed Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend 2.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TissueMend Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiMend PRS Recalled by TEI Biosciences, Inc. Due to Possible out of...
The Issue: Possible out of specification endotoxin test results due to issues with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenylephrine HCl 20 mg added to 0.9% Sodium Chloride 250mL Bag Recalled by...
The Issue: Product Mix up; Product was compounded in 250 mL 5% Dextrose instead of 250...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pain Reliever Recalled by Aurobindo Pharma USA Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: firm's investigation due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Pyxis CII Safe Recalled by CareFusion 303, Inc. Due to Automated...
The Issue: Automated dispensing cabinet devices plugged into any multi-socket outlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-10 Recalled by...
The Issue: There are potential risks of the Hemospray powder adhering to the distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemospray Endoscopic Hemostat: Part Numbers: a) HEMO-7 Recalled by...
The Issue: There are potential risks of the Hemospray powder adhering to the distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nafcillin for Injection Recalled by Sagent Pharmaceuticals Inc Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UroPass Ureteral Access Sheaths Recalled by Olympus Corporation of the...
The Issue: Dilator tips may break in the package and in patients during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviCare Patient Safety V3.9.200 to 3.9.600 Recalled by Baxter Healthcare...
The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voalte Patient Safety Recalled by Baxter Healthcare Corporation Due to...
The Issue: Baxter identified a potential risk where the "safety" monitoring and "bed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW Endurance Extended Dwell Peripheral Catheter System Recalled by ARROW...
The Issue: Potential for catheter separation or leakage
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.