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. 1,135 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,135 in last 12 months

Showing 3681–3700 of 29,425 recalls

Medical DeviceJune 20, 2024· Luminex Corporation

Recalled Item: Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test Recalled by...

The Issue: Potential for defective test cartridges which may result in false positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...

The Issue: If blood culture identification panel is used in conjunction with specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Angiodynamics, Inc.

Recalled Item: SOFT-VU KUMPE 5F X 40CM -Used for patients in need Recalled by...

The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Embecta Corp.

Recalled Item: BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count Recalled by Embecta Corp. Due...

The Issue: BD Nano 2nd Gen Pen Needle was shipped close to or after the labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Angiodynamics, Inc.

Recalled Item: SOFT-VU KUMPE 5F X 65CM -Used for patients in need Recalled by...

The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Foundation Medicine, Inc.

Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...

The Issue: Two (2) reports were sent to customers with an incorrect negative claim on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· Megadyne Medical Products, Inc.

Recalled Item: Brand Name: MEGADYNE" MEGA SOFT" Reusable Patient Return Electrode Product...

The Issue: To limit the use of the Mega Soft Pads to patients aged 12 or older to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2024· Medtronic Neuromodulation

Recalled Item: Medtronic Handset with Communicator Recalled by Medtronic Neuromodulation...

The Issue: A subset of the handsets within the kit may not be able to complete the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat SPACE PUMP IV SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat SPACE PUMP IV SET W/2 CARESITE Recalled by B. Braun Medical, Inc....

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: OUTLOOK IV SET 15DROP W/3 CARESITE-Used with an electrically-powered...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DROP PUMP SET W/2 CARESITE CV- Used Recalled by B. Braun...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DR PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat SPACE PUMP IV SET 15D Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV. 15 DROP PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV.15DROP PUMP SET W/3 SAFELINE LL-Used with an...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2024· B. Braun Medical, Inc.

Recalled Item: Infusomat UNIV 60 DROP PUMP SET Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for the backcheck valve to malfunction, resulting in backflow of...

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

Class II — Potential Health HazardOngoing