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. 2,803 recalls have been distributed to Virginia in the last 12 months.
Showing 9641–9660 of 53,829 recalls
Recalled Item: ICD-DR DDMB1D4 EVERA MRI XT IS-1/DF4 US Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD COBALT VR MRI IS1 DF1 Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRTD DTPA2D1G COBALT XT HF QUAD OUS Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRT-D DTBB2Q1 VIVA QUAD S IS4/DF1 INTL Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRT-D DTBA2D4 VIVA XT IS1/DF4 INTL Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walnut Wearable Smart Thermometer Recalled by BearCare, Inc. Due to There...
The Issue: There have been reports of skin burns to children wearing the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: buPROPrion Hydrochloride Extended-Release Tablets Recalled by SUN...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium Recalled by B. Braun Medical Inc Due to Subpotent: Low...
The Issue: Subpotent: Low anti-factor IIa Potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QIAstat-Dx¿ Respiratory SARS-CoV-2 Panel -IVD intended for the detection and...
The Issue: If cartridges of the affected Serial numbers (SNs) are used, in most cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: vRad PACS with Mammography Recalled by Virtual Radiologic Corp. Due to The...
The Issue: The error resulted in intermittent failure of current (primary) radiology...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylprednisolone Acetate Injectable Suspension Recalled by Amneal...
The Issue: Labeling: Not Elsewhere Classified; A typographical error was observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 20-in vitro diagnostic use only....
The Issue: Potential to cause biased results in the upper end of the reportable range...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducer Kit Recalled by Galt Medical Corporation Due to Sheath...
The Issue: Sheath introducer assemblies could potentially, due to improper storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Defibrillator/pacemaker module (DPM) may encounter a problem causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducer Set Recalled by Galt Medical Corporation Due to Sheath...
The Issue: Sheath introducer assemblies could potentially, due to improper storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LANCASTER SPINACH Recalled by Lancaster Foods LLC Due to Potential Listeria...
The Issue: Possible contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GIANT CURLY LEAF SPINACH Recalled by Lancaster Foods LLC Due to Potential...
The Issue: Possible contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROBINSON FRESH COLLARD GREENS Recalled by Lancaster Foods LLC Due to...
The Issue: Possible contamination with listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROBINSON FRESH KALE GREENS Recalled by Lancaster Foods LLC Due to Potential...
The Issue: Possible contamination with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: bellavista 1000e Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...
The Issue: Vyaire Medical identified two patient safety risks during the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.