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. 2,622 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,622 in last 12 months

Showing 66216640 of 47,654 recalls

Medical DeviceJanuary 16, 2024· Olympus Corporation of the Americas

Recalled Item: Water Filter MAJ-2318. This MAJ-2318 water filter has been designed Recalled...

The Issue: Water filter may have been assembled incorrectly, resulting in unfiltered...

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

Class II — Potential Health HazardOngoing
DrugJanuary 15, 2024· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Phenoxybenzamine Hydrochloride Capsules Recalled by Amneal Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 15, 2024· Medical Action Industries, Inc. 306

Recalled Item: IV Start Kit Recalled by Medical Action Industries, Inc. 306 Due to The kits...

The Issue: The kits contain saline flush syringes which were recalled by the supplier.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2024· D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)...

The Issue: When using those products you may experience difficulties to extend or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2024· D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)...

The Issue: When using those products you may experience difficulties to extend or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2024· D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)...

The Issue: When using those products you may experience difficulties to extend or...

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

Class II — Potential Health HazardOngoing
FoodJanuary 12, 2024· Wegmans Food Markets, Inc.

Recalled Item: 24ct Petite Pastry Tray Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product contains undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 12, 2024· Wegmans Food Markets, Inc.

Recalled Item: Ready To Bake Chocolate and Almond Variety Pk () Recalled by Wegmans Food...

The Issue: Product contains undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 12, 2024· Wegmans Food Markets, Inc.

Recalled Item: 9 oz 10pk Assorted Mini Danish Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product contains undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 12, 2024· Wegmans Food Markets, Inc.

Recalled Item: Ready To Bake Double Chocolate Croissant () Recalled by Wegmans Food...

The Issue: Product contains undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 12, 2024· Wegmans Food Markets, Inc.

Recalled Item: 5 oz 2pk Chocolate Croissant Recalled by Wegmans Food Markets, Inc. Due to...

The Issue: Product contains undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 12, 2024· Neptune Resources, LLC

Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...

The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 12, 2024· Neptune Resources, LLC

Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...

The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 12, 2024· Neptune Resources, LLC

Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...

The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 11, 2024· Amerisource Health Services LLC

Recalled Item: Rifampin Capsules USP Recalled by Amerisource Health Services LLC Due to...

The Issue: Failed Impurities/Degradation Specification.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2024· Par Sterile Products LLC

Recalled Item: Vasostrict (vasopressin in 5% Dextrose) Injection Recalled by Par Sterile...

The Issue: Superpotent Drug: Assay from the 3-month and 6-month stability intervals...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 11, 2024· Micro Therapeutics, Inc.

Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...

The Issue: European version of microcatheter were distributed within US which contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Micro Therapeutics, Inc.

Recalled Item: The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible Recalled...

The Issue: European version of microcatheter were distributed within US which contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2024· Olympus Corporation of the Americas

Recalled Item: Colonoscope Recalled by Olympus Corporation of the Americas Due to Specific...

The Issue: Specific repaired colonovideoscopes were assembled without an adhesive which...

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

Class II — Potential Health HazardOngoing