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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16481–16500 of 27,451 recalls
Recalled Item: AutoCheck5+ Recalled by Radiometer America Inc Due to Radiometer has...
The Issue: Radiometer has recently become aware that a few of the AUTOCHECK 5+ level 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 1000 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 500 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ Recalled by...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intermed 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 5ml Normal Saline (0.9%) Unit Dose¿¿¿¿ ¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex 550 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿¿ ¿¿¿ ¿¿¿...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Prefilled 350 ml Sterile¿¿¿¿ ¿¿¿¿ ¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Unit Dose 5 ml Normal Saline (0.9%)¿¿¿¿ ¿ Recalled by Medex...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intermed 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿¿¿ ¿¿¿ Recalled...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline 300-350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿ ¿ Recalled by...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Unit Dose 15 ml Normal Saline ¿ Recalled by Medex Cardio-Pulmonary...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Prefilled 550 ml Sterile¿¿ ¿ Recalled by Medex Cardio-Pulmonary...
The Issue: Lack of sterility assurance: leaking containers which could lead to exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink H/S Oral Sleep Apnea Device Recalled by Respire Medical Due to...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink H/S Oral Sleep Apnea Device Recalled by Respire Medical Due to...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AERO IOL Injection System containing 10 Z28 Cartridges per box Recalled by...
The Issue: The recommended storage temperature on the label is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink Series EF+ Oral Sleep Apnea Device. Recalled by Respire Medical...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated Peritoneal Dialysis Set with Cassette Recalled by...
The Issue: The firm received increased customer complaints for Missing Red Line,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II Recalled by...
The Issue: There is a potential failure of the top plate assembly, which is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.