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. 1,122 recalls have been distributed to Virginia in the last 12 months.
Showing 8781–8800 of 29,425 recalls
Recalled Item: JAGTOME RX 44-30-260-035 Material Number: M00573060 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 39-30-450-025 Material Number: M00573110 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 44-30-450-035 Material Number: M00573070 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 44-20-450-035 Material Number: M00573050 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 39-30-260-025 Material Number: M00573100 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-30MM/450CM Material Number: M00583070 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 39-20-260-025 Material Number: M00573080 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250 Recalled by...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 49-20MM/450CM Material Number: M00584020 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dreamtome RX Cannulating Sphincterotome-DREAMTOME 44-20MM/260CM Material...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-30-450-035 Material Number: M00573030 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-30-260-035 Material Number: M00573020 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-30MM/260CM Material Number: M00583050 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant Recalled by Medtronic Vascular, Inc. Due to Stent Graft Systems...
The Issue: Stent Graft Systems built with specific batches of taper tip assemblies have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to Potential...
The Issue: Potential cessation in ventilation can occur under specific conditions.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flat Panel Detector Recalled by Canon Medical System, USA, INC. Due to...
The Issue: Abnormal images such as horizontal stripes may be displayed and recovery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm Recalled by Covidien...
The Issue: The firm has received six (6) complaint reports from customers indicating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NobelReplace Conical Connection RP 4.3x11.5 mm STERILE R Recalled by Nobel...
The Issue: Due to 16 complaints related to drivers not engaging in implants. According...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due...
The Issue: 26 Fabius MRI Anesthesia machines were distributed with internal hoses...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20500 Vitale Silver calcium Alginate Dressing Ropes Recalled by CellEra LLC...
The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.