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. 1,026 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
1,026 in last 12 months

Showing 14441–14460 of 47,654 recalls

Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch Recalled by...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 85CB Lotion Ultrasound 8.5 oz 24/cs ECO 40JBC Gel Recalled by National...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheters Recalled by Medtronic Perfusion Systems Due to...

The Issue: Potential for a wire protrusion through the left heart vent catheter tip

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· National Distribution & Contracting Inc

Recalled Item: ECO 50TS Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl Recalled by...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2021· Zhejiang Kindly Medical Devices Co., Ltd.

Recalled Item: McKesson PREVENT HT Safety Blood Collection Needles Recalled by Zhejiang...

The Issue: Potential for difficulty in safety mechanism activation.

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

Class II — Potential Health HazardOngoing
DrugAugust 24, 2021· Efficient Laboratories, Inc.

Recalled Item: Rompe Pecho DM Recalled by Efficient Laboratories, Inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2021· Azurity Pharmaceuticals, Inc.

Recalled Item: Firvanq (vancomycin hydrochloride for oral solution) Recalled by Azurity...

The Issue: Product Mix-up: Incorrect diluent component included in the kit.

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2021· Efficient Laboratories, Inc.

Recalled Item: Rompe Pecho Max Multi-Symptoms Maximum Strength Recalled by Efficient...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2021· Efficient Laboratories, Inc.

Recalled Item: Rompe Pecho Ex Expectorant Recalled by Efficient Laboratories, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2021· Efficient Laboratories, Inc.

Recalled Item: Rompe Pecho CF Cold & Flu Advanced Formula Recalled by Efficient...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2021· Viatris

Recalled Item: Lyrica CR (pregabalin) extended release tablets Recalled by Viatris Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2021· Teligent Pharma, Inc.

Recalled Item: Betamethasone Dipropionate Lotion USP Recalled by Teligent Pharma, Inc. Due...

The Issue: Failed Stability Specifications: lot did not meet specification for the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 23, 2021· Aesthetics Systems Usa Inc

Recalled Item: Action De Gala Recalled by Aesthetics Systems Usa Inc Due to Ultrasound gels...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 20, 2021· Microbiologics Inc

Recalled Item: SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use...

The Issue: The SARS-CoV-2 Process Control (Pellet) contains RNA transcripts that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2021· Microbiologics Inc

Recalled Item: SARS-CoV-2 Process Control (Swab) - Product Usage: intended for use Recalled...

The Issue: The product indicated is contaminated with a plasmid DNA that contains the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2021· Greiner Bio-One North America, Inc.

Recalled Item: Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate Recalled...

The Issue: Complaint of tubes clotting due to variation of anticoagulant and/or tubes...

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

Class II — Potential Health HazardOngoing
DrugAugust 20, 2021· Washington Homeopathic Products, Inc.

Recalled Item: La Core LCL-2-0191 Blend Recalled by Washington Homeopathic Products, Inc....

The Issue: Out-of-specification test results obtained for identification testing based...

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

Class II — Potential Health HazardOngoing
Refund