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. 2,356 recalls have been distributed to West Virginia in the last 12 months.
Showing 29681–29700 of 48,376 recalls
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIVERSAL FLEX2 BREATHING CIRCUIT Recalled by King Systems Corp. dba Ambu,...
The Issue: Potential for leak test failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...
The Issue: Failed Dissolution Specifications; 9 month long term stability
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App versions 2.0.0 Recalled by Roche...
The Issue: A program error (bug) in the Bolus Advisor feature, which could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040...
The Issue: During patient interventions with the urology table the radiation is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Small Particle Aerosol Generator Model SPAG-2 6000 Series (SPAG-2). The...
The Issue: SPAG-2 unit nebulizers from Lot J0571670RA were tested at Next Breath for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Measurement Specialties Reusable Temperature Probe Autoclavable. Sold as...
The Issue: The reusable temperature probes are provided with instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The...
The Issue: The Pause function on central monitors will not automatically resume when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerate Pheno system Recalled by Accelerate Diagnostics Inc Due to Rare...
The Issue: Rare isolates of Enterobacteriaceae may generate a susceptible meropenem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sulfamethoxazole and Trimethoprim Oral Suspension Recalled by Akorn Inc Due...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg Recalled by Meridian...
The Issue: Defective Delivery System; reports of the device failing to activate which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg Recalled by Meridian...
The Issue: Defective Delivery System; reports of the device failing to activate which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Claris Lifesciences Inc...
The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.