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 2881–2900 of 53,829 recalls

Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T R11 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Enterprise 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera CV Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to The...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.0T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2025· Amerisource Health Services LLC

Recalled Item: Voriconazole Tablets Recalled by Amerisource Health Services LLC Due to cGMP...

The Issue: cGMP Deviations: Received notification from their supplier requesting they...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2025· Boston Scientific Corporation

Recalled Item: IceSeed 1.5 CX NEEDLE OUS Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Baxter Healthcare Corporation

Recalled Item: Welch Allyn CONNEX Accessory Power Management Stand: Recalled by Baxter...

The Issue: There were customer reports of devices which experienced battery-related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Boston Scientific Corporation

Recalled Item: IceSeed 1.5 CX NEEDLE US Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Boston Scientific Corporation

Recalled Item: IceSeed 1.5 CX S NEEDLE OUS Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Zimmer, Inc.

Recalled Item: Zimmer Biomet Ceramic Head Recalled by Zimmer, Inc. Due to The associated...

The Issue: The associated product labeling does not adequately provide compatibility...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Boston Scientific Corporation

Recalled Item: IceSeed 1.5 CX S NEEDLE US Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits Recalled by...

The Issue: A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 0.5T Standard Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
FoodMarch 22, 2025· Barry Callebaut USA LLC

Recalled Item: CACAO BARRY Gianduja Noir Recalled by Barry Callebaut USA LLC Due to...

The Issue: Undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2025· GE Medical Systems China Co., Ltd.

Recalled Item: GE Healthcare CARESTATION 750c A2 Recalled by GE Medical Systems China Co.,...

The Issue: GE HealthCare has become aware that certain Carestation 620/650/650c and...

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

Class I — Serious Health HazardOngoing