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. 2,655 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,655 in last 12 months

Showing 34013420 of 47,654 recalls

DrugJanuary 7, 2025· Amerisource Health Services LLC

Recalled Item: Clobazam Tablets Recalled by Amerisource Health Services LLC Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 6, 2025· The Mochi Ice Cream Company

Recalled Item: My Mochi Sorbet Peach Mango Sorbet Recalled by The Mochi Ice Cream Company...

The Issue: Frozen Peach Mango Sorbet contains undeclared allergen (egg)

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 6, 2025· Sysmex America, Inc.

Recalled Item: Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6....

The Issue: Sysmex was made aware of a report of false results due to carry-over caused...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2025· Zimmer, Inc.

Recalled Item: NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E...

The Issue: It was identified internally that two commingle events occurred where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2025· Zimmer, Inc.

Recalled Item: NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C...

The Issue: It was identified internally that two commingle events occurred where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2025· XTANT Medical Holdings, Inc

Recalled Item: Irix-A Integrated Lumbar Fusion System Recalled by XTANT Medical Holdings,...

The Issue: Certain implants in the Irix-A Lumbar Fusion System were distributed while...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2025· LivaNova USA, Inc.

Recalled Item: Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva" Recalled by...

The Issue: Their is a potential that implanted pulse generators may stop delivering...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2025· LivaNova USA, Inc.

Recalled Item: Brand Name: SenTiva DUO" Product Name: VNS Therapy¿ SenTiva DUO" Recalled by...

The Issue: Their is a potential that implanted pulse generators may stop delivering...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2025· Scientia Vascular, Inc.

Recalled Item: Socrates 38 Aspiration Catheter 127 cm length The Recalled by Scientia...

The Issue: Due to manufacturing non-conformance that resulted in channels in the seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2025· US Endodontics, LLC

Recalled Item: Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK...

The Issue: Due to devices being irradiated above the established specification which my...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2025· Beckman Coulter Inc.

Recalled Item: Access PCT Reagent Pack Recalled by Beckman Coulter Inc. Due to Identified...

The Issue: Identified reagent lots are experiencing a high rate of calibration failures...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2025· Belmont Instrument LLC

Recalled Item: Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Recalled...

The Issue: Disposable set may leak during priming from a female quick connector due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 31, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY Recalled by MEDLINE...

The Issue: The catheter subassembly in the Integrated Arterial Catheter was...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 31, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline General Surgery Tray Kits: 1) ARTERIAL LINE INSERTION KIT Recalled...

The Issue: The catheter subassembly in the Integrated Arterial Catheter was...

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

Class I — Serious Health HazardOngoing
FoodDecember 30, 2024· V Chocolates, Inc

Recalled Item: Assorted Chocolate Caramels with kosher sea salt Recalled by V Chocolates,...

The Issue: Small pieces of plastic broken tray in the product.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2024· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP 30 mg Recalled by Rising Pharma...

The Issue: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2024· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine DR Capsules USP 60 mg Recalled by Rising Pharma Holding, Inc. Due...

The Issue: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 30, 2024· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP 20 mg Recalled by Rising Pharma...

The Issue: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 28, 2024· Neilmed Pharmaceuticals Inc

Recalled Item: NeiMed NasoGel for DRY NOSES UDI-DI/code: 00705928045309 SKU...

The Issue: Due to nasal spray stability failure for bioburden.

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

Class II — Potential Health HazardOngoing
DrugDecember 27, 2024· Eugia US LLC

Recalled Item: Progesterone Injection USP Recalled by Eugia US LLC Due to Presence of...

The Issue: Presence of Particulate Matter: A market complaint was received of a glass...

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

Class II — Potential Health HazardOngoing
Refund