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. 2,780 recalls have been distributed to Virginia in the last 12 months.
Showing 11141–11160 of 29,425 recalls
Recalled Item: 9310HD Digital Video Capture Module with software version 3.4.0 or Recalled...
The Issue: There is an intermittent software issue that could affect the systems, in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to There is a potential...
The Issue: There is a potential for a smudge artifact that could be suspect for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray...
The Issue: Potential malfunction in which the examination room monitor may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo XP ProVue Retriever Recalled by Stryker Neurovascular Due to Increase...
The Issue: Increase in fracture complaints of the flexible, tapered core wire,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis (GII) - Product Usage: designed for use in patients Recalled by...
The Issue: The anterior locking detail does not meet its design specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage:...
The Issue: There is a software problem which affects the DSA Roadmap application on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....
The Issue: Device malfunction causing the applier to jam, and clip loading failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Recalled...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9100c NXT system - Product Usage: Device is licensed and Recalled by GE...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is Recalled by...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen Recalled by...
The Issue: Instructions for use in the package insert for SARS Antigen FIA test were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-i Ventilator Recalled by Getinge Group Logistics America, LLC Due to A...
The Issue: A potentially shorter than specified nebulizer connector may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MeritMedical Cultura Flex Swab Recalled by Merit Medical Systems, Inc. Due...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hurricane RX Biliary Balloon Dilatation Catheter Catalog . M00545890...
The Issue: RX tunnel component (black sheath) may detach from the catheter shaft due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.