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. 2,450 recalls have been distributed to West Virginia in the last 12 months.
Showing 18541–18560 of 27,884 recalls
Recalled Item: DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter Inc....
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OEC 9900 Elite mobile fluoroscopy system is designed to Recalled by GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code:...
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN....
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 6800 Recalled by GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The AMM Recalled...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension AMM (DF119)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10 Recalled by Covidien...
The Issue: Labeling error: The label indicates the product is latex free, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT with software version 4.7.0 Product Usage: The Recalled by...
The Issue: Multiple issues have caused the device to result in CT rescans or incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker...
The Issue: The product was not functioning as intended. The ventilation to the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250-Proton Radiation Therapy Product Usage: Proton Radiation Therapy...
The Issue: An error can occur causing Delta corrections to be lost when one setup field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista AMM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Cephalotin CE 256 Foam packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST¿ Ceftriaxone TXL32 SPB Recalled by BioMerieux SA Due to Product...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Fosfomycin FM1024 Blister packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Vancomycin VA 256 FOAM packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Benzyl Penicillin PG256 FOAM packaging Recalled by BioMerieux SA Due...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Ceftazidime TZ256 Foam packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Imipenem IP32 Foam packaging Recalled by BioMerieux SA Due to Product...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST Tobramycin TM256 FOAM packaging Recalled by BioMerieux SA Due to...
The Issue: Product Stability issues: The current shelf-life claims of the ETEST...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.