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. 2,445 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,445 in last 12 months

Showing 3352133540 of 47,654 recalls

FoodFebruary 1, 2016· Geneva Foods, LLC

Recalled Item: Lysander's Premium Teriyaki Marinade Recalled by Geneva Foods, LLC Due to...

The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 1, 2016· Geneva Foods, LLC

Recalled Item: Lysander's All Natural Spicy Bourbon Flavor Rub Recalled by Geneva Foods,...

The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 1, 2016· Geneva Foods, LLC

Recalled Item: Lysander's All Natural Bourbon Flavor Rub Recalled by Geneva Foods, LLC Due...

The Issue: Product contains undeclared allergens soy and wheat. Also does not declare...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge FlexConnect software Recalled by Merge Healthcare, Inc. Due to...

The Issue: Communication protocols interfacing with the affected software version with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: CADstream software. The firm name on the label is Merge Healthcare Recalled...

The Issue: The software was not presenting the PURE filter user interface message on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is an integrated Recalled...

The Issue: Patient information in the header is only found on the first page of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Access used with Merge PACS software provides medical specialists...

The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: iConnect Access used with Ortho PACS software provides medical specialists...

The Issue: Studies that are viewed in iConnect Access that originate on Merge PACS /...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Product was distributed under the AMICAS label Recalled...

The Issue: The patient name in the Halo title bar and the thumbnails do not match the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...

The Issue: A migrated study that has annotations will display the annotations, but when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2016· Merge Healthcare, Inc.

Recalled Item: Merge OfficePACS software. The firm name on the label is Merge Healthcare...

The Issue: Potential data loss occurs as a result of the software archiving not working...

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

Class II — Potential Health HazardOngoing
FoodJanuary 29, 2016· Garden Of Life Llc

Recalled Item: Raw Meal Organic Vanilla Spiced Chai Powder Recalled by Garden Of Life Llc...

The Issue: Products possibly contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 29, 2016· Garden Of Life Llc

Recalled Item: Raw Meal Organic Vanilla Powder Recalled by Garden Of Life Llc Due to...

The Issue: Products possibly contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 29, 2016· Garden Of Life Llc

Recalled Item: Raw Meal Organic Original Powder Recalled by Garden Of Life Llc Due to...

The Issue: Products possibly contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 29, 2016· Garden Of Life Llc

Recalled Item: Raw Meal Organic Chocolate Powder Recalled by Garden Of Life Llc Due to...

The Issue: Products possibly contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 29, 2016· International Tea Importers

Recalled Item: Apple Caramel Almond Tea Recalled by International Tea Importers Due to...

The Issue: International Tea Importers is recalling Apple, Caramel & Almond Tea because...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 29, 2016· Valeant Pharmacueticals International

Recalled Item: Orapharma (Onpharma) Onset Mixing Pen Rx only Recalled by Valeant...

The Issue: It has been determined that the Onset Mixing Pen has an optimal use period...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Corin USA Limited

Recalled Item: Trinity Acetabular Shell Product Usage Total Hip Replacement. Recalled by...

The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Corin USA Limited

Recalled Item: Trinity Acetabular System Product Usage - Total Hip Replacement. Recalled by...

The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2016· Corin USA Limited

Recalled Item: Trinity Acetabular Shell Product Usage: Total Hip Replacement. Recalled by...

The Issue: Potential for abrasion of the sterile barrier pouches of the new packaging...

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

Class II — Potential Health HazardOngoing