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. 2,500 recalls have been distributed to West Virginia in the last 12 months.
Showing 11001–11020 of 27,884 recalls
Recalled Item: AESCULAP S4 Cervical Cross Connector Recalled by Aesculap Implant Systems...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC/DC POWER SUPPLY for 7400 Recalled by ESAOTE S.P.A Due to The AC/DC...
The Issue: The AC/DC adapter (power supply) of the portable ultrasound systems listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC/DC POWER SUPPLY for 7400 Recalled by ESAOTE S.P.A Due to The AC/DC...
The Issue: The AC/DC adapter (power supply) of the portable ultrasound systems listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B. Braun Introcan IV Safety Catheters Recalled by Braxton Medical...
The Issue: Recalled products do not have FDA approval for sale in the United States.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055 Recalled by Biomet, Inc....
The Issue: Product not properly being aligned with the adequate gamma sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055 Recalled by...
The Issue: Product not properly being aligned with the adequate gamma sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Regenerex Primary Taper Cap Item Number 141269 Recalled by Biomet,...
The Issue: Product not properly being aligned with the adequate gamma sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1500 Flex Heat and Moisture Exchanger Recalled by AB ULAX Due to Firm has...
The Issue: Firm has received 6 complaints that the Heat Moisture Exchanger (HME)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet OnPoint SCOPE PROCEDURE KIT Item Number: 24-3050 Recalled by Biomet,...
The Issue: Product not properly being aligned with the adequate gamma sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) RingLoc Bi-Polar Hip System Acetabular Cup ArCom: Acetabular Bi-Polar...
The Issue: Zimmer Biomet is conducting a medical device recall for three lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper...
The Issue: Product potentially being packaged without a taper adapter or baseplate. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 26 IN(66 cm) APPX 3.4ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 42 IN (107 cm) Appx 5.0 ml Recalled by ICU Medical, Inc. Due to Potential...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiros CLOSED MALE LUER w/RED CAP Recalled by ICU Medical, Inc. Due to...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.