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 23012320 of 53,829 recalls

Medical DeviceMay 30, 2025· Maquet Critical Care AB

Recalled Item: Servo-u MR Ventilator System. Model Number: 6888800. Recalled by Maquet...

The Issue: Potential for inaccurate measurement of the patient circuit compliance...

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

Class I — Serious Health HazardOngoing
DrugMay 29, 2025· Eugia US LLC

Recalled Item: Gentamicin Injection Recalled by Eugia US LLC Due to Failed Stability...

The Issue: Failed Stability Specifications: Out of specification results for the Color...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 29, 2025· Macleods Pharmaceuticals Ltd

Recalled Item: Levothyroxine Sodium Tablets Recalled by Macleods Pharmaceuticals Ltd Due to...

The Issue: Presence of a foreign substance: black hair found embedded in tablet.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Achieva Nova-Dual Product Number: 781173 Recalled by Philips...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Explorer/Nova Dual Product Number: 781108 Recalled by Philips...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: SmartPath to dStream for 1.5T¿ Recalled by Philips North America Due to...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Achieva IT Nova Product Number: 781175 Recalled by Philips North...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Achieva Nova Product Number: 781172 Recalled by Philips North...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera Achieva 1.5T Pulsar Recalled by Philips North America Due to...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Master/Nova Product Number: 781106 Recalled by Philips North...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Omni/Stellar Recalled by Philips North America Due to identified...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Achieva XR Product Numbers: (1) 781153 Recalled by Philips North America Due...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

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

Class II — Potential Health HazardOngoing
DrugMay 28, 2025· Apotex Corp.

Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2025· Apotex Corp.

Recalled Item: Azelastine HCl Ophthalmic Solution Recalled by Apotex Corp. Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2025· Pfizer Inc.

Recalled Item: DOBUTamine Injection Recalled by Pfizer Inc. Due to Discoloration;...

The Issue: Discoloration; discolored solution from cracked vials

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2025· Apotex Corp.

Recalled Item: Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution Recalled by Apotex...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 28, 2025· Apotex Corp.

Recalled Item: Lacosamide Oral Solution Recalled by Apotex Corp. Due to Defective...

The Issue: Defective Container: This recall is being initiated due to a leaking unit...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips eL18-4 EMT Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips C9-5EC Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips eL18-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

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

Class II — Potential Health HazardOngoing