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 13011320 of 53,829 recalls

Medical DeviceSeptember 18, 2025· Cook Medical Incorporated

Recalled Item: Zenith Alpha 2 Thoracic Endovascular Graft Recalled by Cook Medical...

The Issue: Affected devices may contain PTFE coating scrapings. Scrapings could be...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2025· Fisher & Paykel Healthcare, Ltd.

Recalled Item: Airvo 2 Recalled by Fisher & Paykel Healthcare, Ltd. Due to When...

The Issue: When unintentionally disconnected from power source, humidifier device (used...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· GE Medical Systems, LLC

Recalled Item: LOGIQ P10 series with software version R4.5.7 Model Number 5877534 Recalled...

The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: Combined Spinal and Epidural Anesthesia Tray 2 Recalled by B BRAUN MEDICAL...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: Combined Spinal and Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL INC...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: ESPOCAN Combined Spinal and Epidural Anesthesia Tray Recalled by B BRAUN...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2025· B BRAUN MEDICAL INC

Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Set Recalled by B BRAUN MEDICAL...

The Issue: Potential for the lid of the catheter connector to be in the incorrect position.

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

Class II — Potential Health HazardOngoing
DrugSeptember 17, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Azelaic Acid Gel Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP...

The Issue: CGMP Deviations: Market complaints received for gritty texture (grainy)

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 17, 2025· Enterix, Inc.

Recalled Item: InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure Recalled...

The Issue: InSure ONE failed sensitivity testing when used with Test Card Lot T241102,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2025· ELEKTA SOLUTIONS AB

Recalled Item: MOSAIQ Oncology Information System Software Builds 3.1.3 Recalled by ELEKTA...

The Issue: When appending a care plan that contains one or more wave medication orders,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2025· Beckman Coulter Inc.

Recalled Item: SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent Recalled by Beckman...

The Issue: Beckman Coulter has identified that there is an increased probability...

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

Class II — Potential Health HazardOngoing