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 2882128840 of 47,654 recalls

Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Willscher Vas Skewers Recalled by Cook Inc. Due to COOK Medical is...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2017· Cook Inc.

Recalled Item: Endoscopic Curved Needle Recalled by Cook Inc. Due to COOK Medical is...

The Issue: COOK Medical is initiating a voluntary recall of multiple products because...

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

Class II — Potential Health HazardOngoing
DrugApril 28, 2017· PAR Sterile Products LLC

Recalled Item: Buprenorphine HCI Injection Recalled by PAR Sterile Products LLC Due to...

The Issue: Crystallization: due to the presence of white, crystalline particulates,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 28, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: TI Transport Monitor/Module Battery Pack Product Usage: intended for...

The Issue: Mindray has received two reports from outside the United States that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2017· KCI USA, INC.

Recalled Item: 1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Recalled...

The Issue: Potential sterile barrier breach

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

Class II — Potential Health HazardOngoing
DrugApril 27, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol Transdermal System) 0.1 mg per day Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for peel force from the...

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

Class III — Low RiskOngoing
Refund
DrugApril 27, 2017· Hetero USA Inc

Recalled Item: Acyclovir Tablets Recalled by Hetero USA Inc Due to Presence of Foreign...

The Issue: Presence of Foreign Substance: human hair melded into tablet.

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

Class III — Low RiskOngoing
Refund
FoodApril 27, 2017· Lords Organics Llc

Recalled Item: Organic Veda brand Ginger Powder Recalled by Lords Organics Llc Due to...

The Issue: Lord Organics is recalling ginger powder because it has the potential to be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing