Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,871 recalls have been distributed to District of Columbia in the last 12 months.
Showing 8521–8540 of 27,451 recalls
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 44-30-260-035 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: NIM TRIVANTAGE EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due...
The Issue: There is potential for multiple issues due to a manufacturing nonconformity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 49-30MM/260CM Material Number: M00583010 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 Cannulating Sphincterotome-DREAMTOME 44-20MM/450CM 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: DREAMTOME 49-30MM/260CM Material Number: M00584010 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: MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors -...
The Issue: The External Retention Bolster contained in the kit may be a larger diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-20MM/260CM Material Number: M00583040 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: RX CHOLANGIOGRAM KIT Material Numbers: M00575241 M00575281 M00575321...
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 39-30-260-025 Material Number: M00584260 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: Universal Chuck-The Universal Chuck is an Instrument Handle provided as...
The Issue: Top cap may loosen and detach if the Universal Chuck becomes jammed and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 44-30MM/450CM Material Number: M00584070 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: 20544 Vitale Silver calcium Alginate Dressings 4x4 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.
Recalled Item: 20548 Vitale Silver calcium Alginate Dressings 4x8 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.