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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,366 in last 12 months

Showing 4534145360 of 47,654 recalls

Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Chek-Stix Combo Pak (Distributed OUS) Catalog Number: 1364E...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens CLINITEK Atlas Positive and Negative Control Strips for Urine...

The Issue: When these lots of control material are reconstituted, the positive control...

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

Class III — Low RiskOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Soft Flow Ang W/L The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Straight Wir The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Str Wire W/L The Sarns Recalled by Terumo Cardiovascular...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Sft Flow Straight The Sarns Aortic Cannula Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 18 Fr 6mm Sft Flow Ang Wire W/L The Sarns Recalled by Terumo Cardiovascular...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 24 Fr 8mm Soft Flow Ang Wire W/L The Sarns Recalled by Terumo Cardiovascular...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 18 Fr 6mm Sft Flow Angled Wire The Sarns Aortic Recalled by Terumo...

The Issue: The presence of plastic flash was identified at the tip of certain lots of...

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

Class II — Potential Health HazardOngoing
FoodNovember 20, 2012· Whole Foods Market

Recalled Item: 365 Organic Orzo Recalled by Whole Foods Market Due to This product (one...

The Issue: This product (one specific lot code) was being held at the manufacturers'...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2012· GE Healthcare It

Recalled Item: The Centricity Laboratory System is intended to be an information Recalled...

The Issue: GE Healthcare is aware of a potential safety issue associated with the use...

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

Class III — Low RiskOngoing
DrugNovember 19, 2012· Ascend Therapeutics Inc

Recalled Item: EstroGel (estradiol gel) 0.06% Recalled by Ascend Therapeutics Inc Due to...

The Issue: Defective Container: Pump head detaching from the canister unit upon removal...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 19, 2012· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Intersept Custom Tubing Pack with or without coating ( Recalled by...

The Issue: Medtronic is initiating an Urgent Medical Device Customer Notification. We...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Roche Diagnostics Operations, Inc.

Recalled Item: Roche COBAS INTEGRA 400 and 400 plus Analyzer Recalled by Roche Diagnostics...

The Issue: A software security issue with Oracles TNS-Listener component has been...

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

Class III — Low RiskOngoing
Medical DeviceNovember 19, 2012· Zimmer, Inc.

Recalled Item: COONMAD/MORREY TOTAL ELBOW ELBOW COMPONENT REPLACEMENT SET BUSHINGS & PINS...

The Issue: Zimmer is initiating a lot specific recall because affected lots could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· BioHorizons Implant Systems Inc

Recalled Item: AutoTac Delivery Handle Recalled by BioHorizons Implant Systems Inc Due to...

The Issue: The cleaning instructions provided may not be sufficient to remove residual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Zimmer, Inc.

Recalled Item: Coonrad/Morrey New Ulnar Revision Kit for Use with Non-Interchangeable...

The Issue: Zimmer is initiating a lot specific recall because affected lots could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· BioHorizons Implant Systems Inc

Recalled Item: Titanium Tack Starter Kit Recalled by BioHorizons Implant Systems Inc Due to...

The Issue: The cleaning instructions provided may not be sufficient to remove residual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Bunnell, Inc.

Recalled Item: Patient Circuit used with the Life Pulse High Frequency Ventilator. Recalled...

The Issue: Customer complaints received indicate the heater wire insulation can melt,...

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

Class I — Serious Health HazardOngoing
FoodNovember 17, 2012· Focus Products Group Llc

Recalled Item: Cocoa~Latte Hot Drink Maker Recalled by Focus Products Group Llc Due to The...

The Issue: The Cocoa~Latte Hot Drink Maker was manufactured with a small brass metal...

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

Class II — Potential Health HazardOngoing
Refund