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 1386113880 of 47,654 recalls

DrugNovember 12, 2021· SterRx, LLC

Recalled Item: dilTIAZem HCl in 5% Dextrose Injection Recalled by SterRx, LLC Due to Lack...

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
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: EPINEPHIrine in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due...

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
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: PHENYLephrine HCl Recalled by SterRx, LLC 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
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: EPINEPHIrine in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due...

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
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Morphine Sulfate in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC...

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
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: NOREPINEPHRINE in 5% Dextrose Injection Recalled by SterRx, LLC Due to Lack...

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
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: 12 HR Allergy & Congestion Relief Fexofenadine HCl Recalled by Dr. Reddy's...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Antihistamine & Nasal Decongestant Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Antihistamine & Nasal Decongestant Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl Recalled...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy & Congestion Relief Allergy Relief D Recalled by Dr. Reddy's...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Recalled...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 12, 2021· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B...

The Issue: Due to a calculation error in the measurement when using 2D trace (manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Philips North America Llc

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2...

The Issue: (1)Start-up problem: Intermittently at start-up of the system, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Invacare Corporation

Recalled Item: Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Recalled by...

The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Invacare Corporation

Recalled Item: Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Recalled by...

The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2021· Invacare Corporation

Recalled Item: Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with Recalled by...

The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...

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

Class II — Potential Health HazardOngoing