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Recalls distributed in District of Columbia

These notices name District of Columbia in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

1,461 stored notices name District of Columbia, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach District of Columbia too — those are in the archive.

Medical devices

Reported Apr 29, 2026

nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft Substitute 90-300-251008: nanOss 3D…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

XTANT Medical Holdings, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beta Bionics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp. (NeuroSciences)

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Reported Apr 8, 2026

" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Jfe Franchising Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2026

MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

BD Alaris" System with Guardrails" Suite MX with Point of Care Unit

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Reported Apr 1, 2026

Favorina Chocolate Ladybugs German-Style Nougat, Net Wt 3.52 oz (100g). UPC 2030 4492. Distributed By Lidl US, LLC,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lidl US TRADING

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2026

MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K/B, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Merit Medical Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 25, 2026

Battery Charging Station; Model: 0998-00-0802;

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Datascope Corp.

FDA (openFDA device enforcement)

Reported Mar 23, 2026

FSIS Issues Public Health Alert for Ground Beef Products Due to Possible Foreign Material Contamination

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

White Oak Pastures

USDA FSIS

Medical devices

Reported Mar 11, 2026

Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Vascutek, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2026

Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2026

MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MRIMed Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-000005-01R , MON-000006 , MON-000006-RFB,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Auris Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN):…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2026

da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 11, 2026

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 4, 2026

Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

LimFlow, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Ireland, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

SQ40S Blood Transfusion Filter

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GVS TM, Inc.

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.