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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,411 in last 12 months

Showing 4134141360 of 47,654 recalls

Medical DeviceJanuary 24, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...

The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...

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

Class II — Potential Health HazardOngoing
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Marshmallow in the following flavors: chocolate Recalled by Araya, Inc Due...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Chocolate Gift Boxes: SC 6 Oreos Recalled by Araya, Inc Due to Undeclared...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Dry fruits covered in chocolate in the following flavors: orange peel...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Chocolate S'mores Araya Artisan Chocolate: 1545 W Grand Parkway S Recalled...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 23, 2014· Araya, Inc

Recalled Item: Gourmet Bar in the following flavors: bacon Recalled by Araya, Inc Due to...

The Issue: Product may contain undeclared allergens

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 23, 2014· Atricure Inc

Recalled Item: Reusable Clip Applier Manufactured by AtriCure Recalled by Atricure Inc Due...

The Issue: The firm was notified by a customer of a cracked spring in the handle of the...

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

Class II — Potential Health HazardOngoing
DrugJanuary 22, 2014· Fresenius Kabi USA, LLC

Recalled Item: Heparin Sodium Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Subpotent; 18 month time point

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 22, 2014· CareFusion 303, Inc.

Recalled Item: SmartSite Needleless Connector Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the SmartSite Needlefree Connector, model number...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2014· Golden Technologies, Inc.

Recalled Item: Buzzaround XL scooters' Product Usage: mobility Recalled by Golden...

The Issue: Buzzaround XL scooters' front to rear lockup can become unintentionally...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2014· Dako North America Inc.

Recalled Item: Product Name: HER2 CISH pharmDx Kit Catalog/Model number: SK109 Recalled by...

The Issue: Dako has initiated a recall of HER2 CISH pharmDxTM Kit because weak red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Multical. ABX PENTRA N Control. ABX PENTRA P Recalled by Horiba...

The Issue: HORIBA Medical is informing all ABX PENTRA MultiCal, N Control, and P...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D and Proteus XR/a equipped with Wireless...

The Issue: GE Healthcare has recently become aware of a software issue associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· Edwards Lifesciences, LLC

Recalled Item: Crimper Model 9100CR26 The Crimper is indicated for use in Recalled by...

The Issue: Edwards Lifesciences is recalling two lot numbers of the 26mm transcatheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2014· Medical Information Technology, Inc.

Recalled Item: MEDITECH Microbiology - Calculator/data processing module Recalled by...

The Issue: Potential for patient results being removed from LAB/EMR.

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

Class II — Potential Health HazardOngoing
DrugJanuary 16, 2014· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Presence of...

The Issue: Presence of Foreign Tablets: A product complaint was received by a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Cooling Eye Drops Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Dry Eye Recalled by The Mentholatum Co. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2014· The Mentholatum Co.

Recalled Item: ROHTO Redness Relief Recalled by The Mentholatum Co. Due to Lack of...

The Issue: Lack of Assurance of Sterility: The Mentholatum Company has recalled Rohto...

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

Class II — Potential Health HazardOngoing
Refund