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. 1,096 recalls have been distributed to Virginia in the last 12 months.
Showing 12861–12880 of 29,425 recalls
Recalled Item: Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive Recalled by Maquet...
The Issue: A loose ODU plug / Coaxial cable connection may result in fluctuating flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healon GV PRO 0.85 mL Recalled by Johnson & Johnson Surgical Vision Inc Due...
The Issue: Ophthalmic viscosurgical device may be difficult to remove from the eye,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer Recalled by GE...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate 3 Mobile Power Unit Recalled by Thoratec Corp. Due to Excessive...
The Issue: Excessive static electricity can potentially cause unrecoverable power loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPince Full Core Biopsy Instrument 16ga x 15cm. Recalled by Argon Medical...
The Issue: Incorrect product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience trays and kits Recalled by Medical Action Industries,...
The Issue: The kits contain a bottle of saline solution which may exceed the USP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CardioChek Starter Kit Recalled by Polymer Technology Systems,...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PuraSinus Absorbable Nasal Hemostat Recalled by 3-D Matrix, Inc. Due to The...
The Issue: The boxes used by the shipper were not validated for use during transport.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickDraw Venous Cannula Recalled by Edwards Lifesciences, LLC Due to If the...
The Issue: If the venous cannula is used in an unintended manner (longer than 6 hours;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-se Fiber Optic Miller 2 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Mac 3 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iMRX MRI and Angiography System Recalled by Deerfield Imaging, Inc. Due to...
The Issue: There is a potential hardware error for the iMRX System with a generator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended...
The Issue: GE Healthcare has become aware that there is a potential for a loose cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to During a...
The Issue: During a routine inspection of a system, a crack on the C-arm holder was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.