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. 1,936 recalls have been distributed to Virginia in the last 12 months.
Showing 21001–21020 of 53,829 recalls
Recalled Item: ROSA One 3.1 Brain Application Recalled by MEDTECH SAS Due to Some...
The Issue: Some cross-sectional images from the image acquisitions of the patients head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ducktrap River of Maine Herring Center Cuts in Wine Sauce Recalled by...
The Issue: Herring in Wine Sauce contains undeclared milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC...
The Issue: When inflating/deflating a single bladder, both bladders could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaginal Verification Panel Lot 8208-11 Recalled by Microbiologics Inc Due to...
The Issue: Product 8208 Vaginal Verification Panel is a 6 pool kit and has contaminant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coated VICRYL (Polyglactin 910) Suture Recalled by Ethicon, Inc. Due to Some...
The Issue: Some sutures in the lot may exhibit a small section of braid fraying, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheters are indicated for the assessment of hemodynamic...
The Issue: Inability for the guidewire to pass through the needles included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075...
The Issue: A mix-up of autosampler tube positions with a possibility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integris Allura 9 Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardio Vascular-Allura Centron Recalled by Philips North America, LLC Due to...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroDiagnost Eleva Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.