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. 1,096 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,096 in last 12 months

Showing 13881–13900 of 29,425 recalls

Medical DeviceJune 10, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView SPECT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: An issue with the handcontroller may result in either spontaneous...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to An...

The Issue: An issue with the handcontroller may result in either spontaneous...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Molded Products Inc

Recalled Item: Luer Lock Set - Catalog # MPC-125 Recalled by Molded Products Inc Due to...

The Issue: Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2019· Olympus Corporation of the Americas

Recalled Item: Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm...

The Issue: WM-NP/DP2 workstations could become unstable and may fall over if the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Thyroid Collar Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Stretch Buckle Closure Apron Recalled by Burlington Medical, LLC Due...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: 2 pc Full Overlap Vest & Kilt Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: 2 pc Full Wrap Vest & Kilt Back-Saver Recalled by Burlington Medical, LLC...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Porta Shield Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Quick Drop OR Apron Recalled by Burlington Medical, LLC Due to The...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Half Apron Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Cap Recalled by Burlington Medical, LLC Due to The protective material used...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Peak Vest Recalled by Burlington Medical, LLC Due to The protective material...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: 1 pc Full Wrap Support Belt Apron Recalled by Burlington Medical, LLC Due to...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: 1 pc Full Wrap Back Relief Apron Recalled by Burlington Medical, LLC Due to...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Frontal Apron with Quick Drop Velcro Closure (no elastic) Recalled by...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Philips North America, LLC

Recalled Item: Philips HeartStart MRx devices in use with the M3539A AC Power Module:...

The Issue: The AC power module may fail at a higher than expected rate. If a fully...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Overlap Vest Recalled by Burlington Medical, LLC Due to The protective...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Vest Recalled by Burlington Medical, LLC Due to The protective material used...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2019· Burlington Medical, LLC

Recalled Item: Hood Recalled by Burlington Medical, LLC Due to The protective material used...

The Issue: The protective material used in the manufacture of the products could...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing