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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,448 in last 12 months

Showing 3036130380 of 47,654 recalls

DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Phenylephrine HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride Recalled...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Morphine Sulfate 1 mg/mL in 0.9% Sodium Chloride Recalled by Cantrell Drug...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 18, 2016· Cantrell Drug Company

Recalled Item: Calcium Chloride 1 g/50 mL* Added to 5% Dextrose (20 mg/mL)* Recalled by...

The Issue: Lack of Assurance of Sterility - the firm is recalling select sterile drug...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 18, 2016· Swissray Medical

Recalled Item: ddR Formula B X-ray System Recalled by Swissray Medical Due to Potential for...

The Issue: Potential for bucky (the part that holds the grid and is moveable to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Incubator Ohmeda Medical Giraffe Incubator-The Giraffe Incubator is...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: CarePlus Incubator Ohmeda-Ohio CarePlus Incubator- Incubators provide a...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Bedded Warmer Recalled by Ohmeda Medical Due to Certain power cords...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe OmniBed Ohmeda Medical Giraffe OmniBed- The OmniBed is a Recalled by...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Spot PT Ohmeda Medical Spot PT Lite Phototherapy System- Recalled by...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Incubator The Giraffe Incubator is an infant incubator. Incubators...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: IWS Infant Warmer System-Infant radiant warmers provide infrared heat...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe OmniBed Ohmeda Medical Omnibed- The OmniBed is a combination...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Ohmeda Medical

Recalled Item: Giraffe Exam Light The Exam Light illuminates body surfaces and Recalled by...

The Issue: Certain power cords could overheat. The affected power cords were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System Recalled by...

The Issue: There's a potential for liquid penetration into the back side of the front...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE/IMMULITE 1000 Systems Prostate-Specific Antigen (PSA) Assay...

The Issue: Siemens Healthcare Diagnostics has confirmed that the IMMULITE/ IMMULITE...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000/IMMULITE 2000 XPi Systems Prostate-Specific Antigen (PSA)...

The Issue: Siemens Healthcare Diagnostics confirmed that the IMMULITE 2000/ IMMULITE...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2016· Teleflex Medical

Recalled Item: WECK Visistat 35W Recalled by Teleflex Medical Due to Sterility Deficiency:...

The Issue: Sterility Deficiency: The packages are not sealed properly and thus the...

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

Class II — Potential Health HazardOngoing
DrugNovember 17, 2016· Tri-Coast Pharmacy

Recalled Item: TriMix Recalled by Tri-Coast Pharmacy Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund