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. 2,584 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,584 in last 12 months

Showing 1160111620 of 27,451 recalls

Medical DeviceApril 30, 2020· Cook Inc.

Recalled Item: Pressure Monitoring Set Recalled by Cook Inc. Due to The Pressure Monitoring...

The Issue: The Pressure Monitoring Set and Tray may contain excess coating material on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Hill-Rom, Inc.

Recalled Item: Centrella Smart+ Bed Recalled by Hill-Rom, Inc. Due to The Bed Exit System...

The Issue: The Bed Exit System may fail to send a remote alert through the nurse call...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Cook Inc.

Recalled Item: Pressure Monitoring Tray Recalled by Cook Inc. Due to The Pressure...

The Issue: The Pressure Monitoring Set and Tray may contain excess coating material on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Premium Urine Meter Foley Tray Recalled by Covidien Llc...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400mL Recalled by Covidien Llc Due to Temperature sensing catheters...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Foley Catheter with Temperature 16FR 5CC2W Recalled by...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Foley Catheter with Temperature Sensor 14FR 5CC2W...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Premium Urine Meter Tray 400mL Recalled by Covidien Llc...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2300 Lifeline/ReviveR View Recalled by Defibtech, LLC Due to A component...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2400EN Lifeline PRO Recalled by Defibtech, LLC Due to A component issue...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Philips North America, LLC

Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A Recalled...

The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing