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. 2,803 recalls have been distributed to Virginia in the last 12 months.
Showing 10301–10320 of 53,829 recalls
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIOX FX25 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...
The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIOX RX15 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...
The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300 Portable Electric Ventilator Recalled by Philips Respironics,...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Portable Electric Ventilator Recalled by Philips...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 and LifeVentEVO2 Portable Electric Ventilator Recalled by...
The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4...
The Issue: Not able to achieve desired pressure and not holding pressure result from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use for the following Leksell Stereotactic System and...
The Issue: The incorrect IFU was distributed with the devices.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Express Mini 500 Dry Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Color Cuff Single Port Recalled by Stryker Sustainability Solutions Due to...
The Issue: Increased incidence of disposable tourniquet cuffs "not able to achieve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...
The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Labeling: Not elsewhere classified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Russel Stover Sugar Free Peanut Butter Cups packaged in 2.4oz peg bag...
The Issue: Outer package is mislabeled and does not declare tree nuts (pecans).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Omega Medical Imaging Elevating Monitor Suspension Recalled by Omega Medical...
The Issue: An actuator separated from the pivot mechanism on a lower monitor boom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to APLS IgM reagent...
The Issue: APLS IgM reagent kits were packaged with the incorrect conjugate, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM Recalled by...
The Issue: The external diameter of the biopsy instrument is larger than the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...
The Issue: Re-optimization, after adding contours without forced density outside the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.