Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,047 recalls have been distributed to Virginia in the last 12 months.
Showing 18781–18800 of 53,829 recalls
Recalled Item: Lidl Organic Butter Microwave Popcorn Recalled by Lidl US TRADING Due to...
The Issue: Lidl US, LLC has initiated a recall of Lidl Organic Butter Microwave...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lightly salted microwave popcorn packaged in the following ways: 1) Recalled...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Light microwave popcorn packaged in the following ways: 1) Full Recalled by...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: AESCULAP S4 Cervical Cross Connector L 28-33mm Recalled by Aesculap Implant...
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: AESCULAP S4 Cervical Cross Connector L24mm Recalled by Aesculap Implant...
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: AESCULAP S4 Cervical Cross Connector L22mm Recalled by Aesculap Implant...
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: 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: AESCULAP S4 Cervical Cross Connector L 42-58mm Recalled by Aesculap Implant...
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: AESCULAP S4 Cervical Cross Connector L 33-42mm Recalled by Aesculap Implant...
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: Buprenorphine Transdermal System 5 mcg/hour Recalled by Teva Pharmaceuticals...
The Issue: Failed Stability Specifications: Below specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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 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.