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. 1,122 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
1,122 in last 12 months

Showing 9381–9400 of 53,829 recalls

Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iR Recalled by Maquet Medical Systems USA Due to 1. An accessory may...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: BEQ-HMOD70000-USA/QUADROX-iD Recalled by Maquet Medical Systems USA Due to...

The Issue: 1. An accessory may be improperly placed during packaging, causing creases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-iD Pediatric Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· Maquet Medical Systems USA

Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to Product...

The Issue: Product packaging may exhibit small pinholes which may not be visible to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...

The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...

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

Class II — Potential Health HazardOngoing
FoodMay 17, 2023· HU PRODUCTS

Recalled Item: Hu Vanilla Crunch Dark Chocolate bar Recalled by HU PRODUCTS Due to...

The Issue: may contain undeclared tree-nuts

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 16, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Aptio Automation Storage and Retrieval Module (SRM) Recalled by Siemens...

The Issue: A firmware error may lead to an incorrect association of test result(s) to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Bryan Medical Inc

Recalled Item: Aeris Balloon Dilation Catheter Recalled by Bryan Medical Inc Due to Mislabeling

The Issue: Devices were mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Heartware, Inc.

Recalled Item: HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech...

The Issue: Medtronic has identified that the logfiles downloaded from the recently...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2023· Draeger Medical Systems, Inc.

Recalled Item: Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale...

The Issue: The Resuscitaire Infant Radiant Warmer with the optional scale could display...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· Olympus Corporation of the Americas

Recalled Item: Always-On Tip Tracked Instruments (SPiN Drive instruments) Triple Needle...

The Issue: Electromagnetic (EM) sensor tracking malfunction impacts the use of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· NeuMoDx Molecular Inc

Recalled Item: NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of...

The Issue: Potential for lot number discrepancies between the test strip packaging and...

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

Class III — Low RiskOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing