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. 2,849 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,849 in last 12 months

Showing 861880 of 29,425 recalls

Medical DeviceSeptember 26, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: CODMAN Disposable Perforator 11mm. Cranial Perforator. Recalled by Integra...

The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: CODMAN Disposable Perforator 9mm. Cranial Perforator. Recalled by Integra...

The Issue: Expansion of recall of size 14 mm Codman Disposable Perforators for...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 26, 2025· Synthes (USA) Products LLC

Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...

The Issue: Although the etched length on the screw is correct, the length marked on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2025· Synthes (USA) Products LLC

Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...

The Issue: Although the etched length on the screw is correct, the length marked on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· DJO, LLC

Recalled Item: Cold Form Wrap: Back Recalled by DJO, LLC Due to The IFU (Information for...

The Issue: The IFU (Information for Use) on the wrap instructs the user to heat the hot...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...

The Issue: A manufacturing issue could lead to a malformed cover tube press which can...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· Covidien, LP

Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...

The Issue: A manufacturing issue could lead to a malformed cover tube press which can...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· PHILIPS MEDICAL SYSTEMS

Recalled Item: Model: Incisive CT for Brazil SKD Recalled by PHILIPS MEDICAL SYSTEMS Due to...

The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· PHILIPS MEDICAL SYSTEMS

Recalled Item: Model: CT 5300 Recalled by PHILIPS MEDICAL SYSTEMS Due to Issue 1: The...

The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2025· PHILIPS MEDICAL SYSTEMS

Recalled Item: Model: Incisive CT Recalled by PHILIPS MEDICAL SYSTEMS Due to Issue 1: The...

The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2025· Stryker Sustainability Solutions

Recalled Item: HARMONIC FOCUS Shears + Adaptive Tissue Technology Recalled by Stryker...

The Issue: Due to manufacturing issue, reprocessed shears, may become stuck in the "on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2025· Aesculap Inc

Recalled Item: Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER...

The Issue: It was determined there is the potential of silicone fragments detaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2025· Aesculap Inc

Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...

The Issue: It was determined there is the potential of silicone fragments detaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2025· Aesculap Inc

Recalled Item: Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Recalled...

The Issue: It was determined there is the potential of silicone fragments detaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2025· Aesculap Inc

Recalled Item: Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Recalled...

The Issue: It was determined there is the potential of silicone fragments detaching...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2025· Total Joint Orthopedics, Inc.

Recalled Item: Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic...

The Issue: Potential packaging issue that could compromise the sterile barrier. Defect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2025· Becton Dickinson & Co.

Recalled Item: BD Veritor Connect Software Recalled by Becton Dickinson & Co. Due to...

The Issue: Product service credentials used by some BD technical support teams to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2025· Becton Dickinson & Co.

Recalled Item: BD EpiCenter Microbiology Data Management System Recalled by Becton...

The Issue: Product service credentials used by some BD technical support teams to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2025· Becton Dickinson & Co.

Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...

The Issue: Product service credentials used by some BD technical support teams to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2025· Becton Dickinson & Co.

Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...

The Issue: Product service credentials used by some BD technical support teams to...

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

Class II — Potential Health HazardOngoing