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. 2,848 recalls have been distributed to Virginia in the last 12 months.
Showing 1961–1980 of 53,829 recalls
Recalled Item: BritePro Solo Mini with Pro Miller Blade Size 1.5 Recalled by Flexicare...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BritePro Solo Single-Use Fiber Optic Laryngoscope Handle :040-310AU and...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle Recalled by...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BritePro Solo Single-Use Fiber Optic Handle and Blade : 040-331U (Mac 1)...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle Recalled by...
The Issue: Laryngoscope handles may not illuminate as intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Agar Recalled by Remel, Inc Due to Potential Listeria Contamination
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood/MacConkey Biplate 100/PK Recalled by Remel, Inc Due to Potential...
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Strep Selective II Agar Recalled by Remel, Inc Due to Potential Listeria...
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood/EMB Recalled by Remel, Inc Due to Potential Listeria Contamination
The Issue: The products may contain surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bicillin L-A (penicllin G benzathine injectable suspension) Recalled by...
The Issue: CGMP Deviations; particulates identified during visual inspection
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bicillin L-A (penicillin G benzathine injectable suspension) Recalled by...
The Issue: CGMP Deviations; particulates identified during visual inspection
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beauty & Skincare Power Stick original nourishing invisible protection...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shave and Skincare Power Stick Original Nourishing Invisible Protection...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative Recalled by...
The Issue: FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MICRO-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Joystick R-net. Electrical wheelchair component. Recalled by mo-Vis...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All-round Joystick R-net Light. Electrical wheelchair component. Recalled by...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-MULTI-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due to...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDM-ARLITE-R. Electrical wheelchair component. Recalled by mo-Vis BVBA Due...
The Issue: Devices with firmware versions 2.3 and lower may experience timing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.