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. 1,921 recalls have been distributed to Virginia in the last 12 months.
Showing 24921–24940 of 29,425 recalls
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Linear Accelerators of type ARTISTE Recalled by Siemens Medical...
The Issue: A safety risk exists with automatically sequenced treatment technique using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abacus 3.1 Recalled by Baxter Corporation Englewood Due to Baxter...
The Issue: Baxter Corporation is initiating a field correction following an upgrade to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheters Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner catheter of some Langston V2 Dual Lumen Catheters have separated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FirmArray Blood Culture Identification (BCID) Panel Recalled by BioFire...
The Issue: BioFire has identified an increased risk of false positive results when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Although the Natural Rubber Latex...
The Issue: Although the Natural Rubber Latex caution symbol is clearly displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Dual-stage Venous Return Cannulae 28/38 Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer M/L Taper Hip Stem Standard & Extended Offset Recalled by Zimmer,...
The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB Catheter Kit Product Usage: Venous Return Cannula is indicated Recalled...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Cardiovascular Systems Recalled by Cardiovascular Systems, Inc. Due to...
The Issue: CSI has initiated a recall on the Diamondback 360 Peripheral Orbital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Malleable Venous Return Cannulae 24 Recalled by Terumo Cardiovascular...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Flexible Aortic Arch Cannula 8.0mm with luer Recalled by Terumo...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Two-stage Venous Return Cannulae 32/40 & 36/51 Fr with Recalled by...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Soft-Flow Aortic Cannulae 6.0mm Recalled by Terumo Cardiovascular...
The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Potential loss of airway...
The Issue: Potential loss of airway gas measurement in the Compact Airway Gas Modules....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.