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.

53,829 total recalls
2,848 in last 12 months

Showing 23212340 of 29,425 recalls

Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXperFD20/10 System Code: (1) 722029 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) Recalled by PHILIPS...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXperFD20/15 System Code: (1) 722058 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 5 M12 System Code: (1) 722227 (2) 722231 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026 Recalled by PHILIPS...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/20 System Code: (1) 722038 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280 Recalled by...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 Recalled...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10C System Code: (1) 722001 Recalled by PHILIPS MEDICAL...

The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis: MedFlex Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing device labeling is being updated to strengthen labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2025· Spectranetics Corporation

Recalled Item: Intact Vascular Tack Endovascular System Recalled by Spectranetics...

The Issue: Use of Tack Endovascular system, designed to treat acute dissections of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2025· Integra LifeSciences Corp.

Recalled Item: Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Recalled by...

The Issue: Potential that the induction seal is not completely sealed to the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2025· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Large Volume Pump Software, version 5.9.2 and earlier has potential for the...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2025· Nobel Biocare

Recalled Item: . Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Recalled by Nobel Biocare...

The Issue: Due to manufacturing issue (unintended by-product of the injection molding...

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

Class II — Potential Health HazardOngoing