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.
1,479 stored notices name District of Columbia, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach District of Columbia too — those are in the archive.
Reported Mar 1, 2017
ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Discovery MR450 The systems are whole body magnetic resonance scanners designed to support high resolution, high…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Feb 22, 2017
BrightView XCT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Whole Foods Market, TART FRESH FRUIT AMERO SHELL LARGE
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market Brand 365, LLC
7 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 15, 2017
Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Everroast Chicken Caesar Wrap, UPC: 72036-95828, in clear flexible plastic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Harris Teeter
FDA (openFDA food enforcement)
Reported Feb 1, 2017
Hitachi Oasis MRI System - C-Spine Coil
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Mallinckrodt Pharmaceuticals INOmax DSIR Plus delivery system. Model 10007. Delivers INOMAX (nitric oxide for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INO Therapeutics (dba Ikaria)
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Femoral and Tibial Cutting Block Adapter Base. Brainlab knee, BrainLAB Image Guided Surgery System / Instrument,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Amplia MRI" CRT -D SureScan", Amplia MRI" Quad CRT -D SureScan", Claria MRI" CRT -D SureScan", Claria MRI" Quad CRT -D…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc., Cardiac Rhythm and Heart Failure
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 11, 2017
G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180-07, 9180-17, 9101-00, 9101-06…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Interventional Spine Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Innova 2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
CyberKnife Robotic Radiosurgery Systems, models: G3, G4, VSI. Radiology: The CyberKnife Robotic Radiosurgery System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Fresh Express Kit Caesar salad, Net Wt. 7.6 oz. (215g), Fresh Express Incorporated, 550 S. Caldwell St. Charlotte, NC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Express Incorpated
FDA (openFDA food enforcement)
Reported Dec 21, 2016
Apple Tree Goat Dairy Chevre, Net Wt. 8 oz. shrink wrap and wt. 5 lb blocks, Richfield, PA 17086.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Apple Tree Goat Dairy
4 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 21, 2016
Cook Spectrum Minocycline/Rifampin Impregnated Double Lumen Central Venous Catheter Tray Cook Spectrum…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2016
GE Healthcare, Avance, Avance CS2, Amingo.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides phototherapy underneath the infant and can be used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Performance-LOAD Ambulance Cot Fastener Stretcher, Wheeled
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
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.