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. 2,848 recalls have been distributed to Virginia in the last 12 months.
Showing 3141–3160 of 29,425 recalls
Recalled Item: AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU Recalled...
The Issue: Labeling Correction: Instructions For Use (IFU)-Updated electronic Rev 5,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001 Recalled by Kinova...
The Issue: Potential installation issue that could result in a fire hazard in the event...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation S8 App versions 1.3.0 and 1.3.2 Recalled by Medtronic...
The Issue: Due to two software anomalies that can occur within a spine procedure. Two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healgen Series Reagent strips for Urinalysis are composed of several...
The Issue: The reason for this recall is Healgen Scientific Ltd. has determined that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 Recalled by PHILIPS...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Recalled by...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Name: 708038 MultiDiagnost Eleva with Flat Detector 708037...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci 5 Recalled by Intuitive Surgical, Inc. Due to Surgical system Error...
The Issue: Surgical system Error 23062 due to connector1) Partially damaged "Potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Gastrointestinal Videoscope Recalled by Olympus Corporation of the...
The Issue: It was discovered during device performance testing that the CCD imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Cardiology Hemo. Version 12.2. Recalled by CHANGE HEALTHCARE CANADA...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortera Spinal Fixation System Screw Recalled by XTANT Medical Holdings, Inc...
The Issue: Spinal fixation system implant screws marked "DNI" are not intended to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemo. Versions 14.2 Recalled by CHANGE...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo. Versions 13.0 Recalled by CHANGE HEALTHCARE CANADA...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...
The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...
The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miami J Select Collar Recalled by Ossur H / F Due to Pressure sensitive...
The Issue: Pressure sensitive adhesive hooks attached to the sides of the anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BinaxNOW Respiratory Strep A Test Kit Recalled by Cypress Medical Products...
The Issue: Due to a classification error in our inventory management system, these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.