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.
Reported Apr 6, 2022
MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
FDA (openFDA device enforcement)
Reported Apr 6, 2022
Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N 10263 or P/N 37808)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mevion Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2022
RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RaySearch America Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2022
Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2022
Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2022
Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fdmr, Inc. dba Suji's Korean Cuisine
FDA (openFDA food enforcement)
Reported Mar 23, 2022
14" Raw Buttermilk Breakfast Tart with Cranberries, Apples & Granola P2004 (9 Frozen Pancakes). Barcode:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gourmet Kitchen, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 23, 2022
Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2022
Mycoplasma genitalium Control Panel (Inactivated Pellet)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2022
CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec, Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2022
Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Factor
FDA (openFDA food enforcement)
Reported Mar 9, 2022
Alinity m Integrated Reaction Units (IRU)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acorn Stairlifts, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Favorite Day Carrot cake soft bake cookies Net Wt 8 oz. (227g) UPC 0 885239 25803 3 packaged in gable top carton 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J & M Foods, Inc.
FDA (openFDA food enforcement)
Reported Mar 9, 2022
Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial Verification Panel (Inactivated Pellet)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2022
Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2022
IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neuroworks/Sleepworks software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Feb 23, 2022
bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. The bellavista…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
FDA (openFDA device enforcement)
Reported Feb 2, 2022
GE Vscan Extend, being sold as "Vscan Extend Console"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 26, 2022
VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jan 26, 2022
ZOCALO AJI LIMO DRIED CHILI PODS- ORGANIC, Dried Aji Peppers for consumer consumption. Product is vacuum sealed in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Power Selles Imports dba Culinary Collective
FDA (openFDA food enforcement)
Reported Jan 12, 2022
Simplexa Direct Amplification Disc Kit, Product Kit Code MOL1455
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
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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.