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 2788127900 of 47,654 recalls

FoodJune 14, 2017· Wildway LLC

Recalled Item: Wildway Apple Cinnamon Grain-Free Granola 8 oz and 10 oz Recalled by Wildway...

The Issue: Potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 14, 2017· New England Natural Bakers, Inc.

Recalled Item: New England Natural Bakers Organic Muesli -5lb and 25 lb. Recalled by New...

The Issue: Product may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 14, 2017· Wildway LLC

Recalled Item: Wildway Coconut Cashew Grain-free Granola 8 oz. and 10 oz. Recalled by...

The Issue: Potential to be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 14, 2017· New England Natural Bakers, Inc.

Recalled Item: Millville Fruit & Nut Whole Grain Granola - 16 oz Recalled by New England...

The Issue: Product may be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 14, 2017· GoMacro, Inc.

Recalled Item: go macro THRIVE Chocolate Recalled by GoMacro, Inc. Due to Potential...

The Issue: GoMacro is recalling specific MacroBars and Thrive Bars because they may be...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy¿ AspireHC¿ Generator Recalled by Cyberonics, Inc Due to...

The Issue: Manufacturing process used to assemble the circuit board may result in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2017· Cyberonics, Inc

Recalled Item: VNS Therapy¿ AspireHC¿ Generator Recalled by Cyberonics, Inc Due to...

The Issue: Manufacturing process used to assemble the circuit board may result in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Invuity, Inc.

Recalled Item: INVUITY(R) PhotonBlade(TM) Recalled by Invuity, Inc. Due to A small number...

The Issue: A small number of customer observations were recently received which related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· CareFusion 303, Inc.

Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to BD initiated the...

The Issue: BD initiated the recall of Alaris PC unit model 8015 after the firm...

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

Class II — Potential Health HazardOngoing
DrugJune 12, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Gaviscon (Alumina & Magnesium Trisilicate) Regular Strength Original Flavor...

The Issue: Superpotent Drug: high out-of-specification result for magnesium.

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

Class III — Low RiskOngoing
Refund
DrugJune 12, 2017· Vi-Jon, Inc.

Recalled Item: Magnesium Citrate Saline Laxative Cherry Flavored Recalled by Vi-Jon, Inc....

The Issue: Presence of foreign substance: glass particle

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Recalled by...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva II Meter - Product Usage: a. The Accu-Chek Recalled by Roche...

The Issue: Meters may contain a damaged C29 capacitor resulting in issues with power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Sorter 9tray Recalled by Tosoh Bioscience Inc Due to This recall has...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2017· Tosoh Bioscience Inc

Recalled Item: Tosoh¿Automated Enzyme Immunoassay Analyzer AIA-900 Recalled by Tosoh...

The Issue: This recall has been initiated due to a potential malfunction of the photo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2017· Kelyniam Global, Inc.

Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...

The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2017· Sorin Group USA, Inc.

Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...

The Issue: Identification of excess plastic on the tip of the cannula.

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

Class II — Potential Health HazardOngoing