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. 2,813 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,813 in last 12 months

Showing 66016620 of 29,425 recalls

Medical DeviceMay 2, 2023· Smith & Nephew, Inc.

Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...

The Issue: Recent complaint data indicates that the revision rate may be trending...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2023· Smith & Nephew, Inc.

Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...

The Issue: Recent complaint data indicates that the revision rate may be trending...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2023· Smith & Nephew, Inc.

Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...

The Issue: Recent complaint data indicates that the revision rate may be trending...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 EV300 Recalled by Philips Respironics, Inc. Due to...

The Issue: Environmental debris may accumulate on the internal machine flow sensor...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2023· Becton Dickinson & Co.

Recalled Item: BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B Recalled by...

The Issue: IFU- Instructions for Use (IFU) package insert and both the IFU packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Environmental...

The Issue: Environmental debris may accumulate on the internal machine flow sensor...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...

The Issue: The Trilogy Evo Universal ventilator provides continuous or intermittent...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 and LifeVent EVO2 Recalled by Philips Respironics, Inc. Due...

The Issue: Environmental debris may accumulate on the internal machine flow sensor...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 28, 2023· Qiagen Sciences LLC

Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel multiplexed nucleic acid real-time...

The Issue: Faulty cartridges in the lot could result in false test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2023· NRT X-RAY A/S

Recalled Item: Intelli-C Recalled by NRT X-RAY A/S Due to There is a potential that the...

The Issue: There is a potential that the drive shaft in the detector up/down (IDE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2023· NRT X-RAY A/S

Recalled Item: Intelli-C Recalled by NRT X-RAY A/S Due to There is a potential that the...

The Issue: There is a potential that the drive shaft in the detector up/down (IDE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2023· HeartSine Technologies Ltd

Recalled Item: HeartSine Recalled by HeartSine Technologies Ltd Due to Single use battery...

The Issue: Single use battery and electrode cartridge may be rendered inoperable due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· BioFire Diagnostics, LLC

Recalled Item: FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 &...

The Issue: The firm has identified an increased risk of obtaining false positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT-Computed Tomography X-Ray System Model: 728143 Recalled by...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT Power (China)-Computed Tomography X-Ray System Model: 728148...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT Plus-Computed Tomography X-Ray System Model: 728149 Recalled by...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Davol, Inc.

Recalled Item: Ventralight ST w Echo PS 4.5" Circle A low profile Recalled by Davol, Inc....

The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Davol, Inc.

Recalled Item: Ventralight ST w EchoPS 4"x6" Ellipse- A low profile Recalled by Davol, Inc....

The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Davol, Inc.

Recalled Item: Ventralight ST 4.5" Circle with Echo PS- A low profile Recalled by Davol,...

The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...

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

Class II — Potential Health HazardOngoing