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 Mar 25, 2015
SMOKED NOVA Salmon, NET WT 4 oz (113g). Product is held in vacuum packs with black, beige and yellow labeling.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Acme Smoked Fish Corp.
FDA (openFDA food enforcement)
Reported Mar 25, 2015
Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2015
Juno DFR X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
FDA (openFDA device enforcement)
Reported Mar 11, 2015
DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iCAD, Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2015
HeartWare Ventricular Assist System (HeartWare Controller) Product Usage: For use as a bridge-to-cardiac…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
TDX Electric Wheelchair. Invacare FDX, TDX series and Storm Series (3G) power wheelchairs in 20 to 24 inch width…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Medtronic, Quadripolar ITREL 3 IPG, Model 7425, is a multiprogrammable device designed for use in the Stimulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Feb 25, 2015
This correction applies to all GE Healthcare MRI systems with superconducting magnets: Discovery MR450, Discovery…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare
FDA (openFDA device enforcement)
Reported Feb 18, 2015
The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corporation
FDA (openFDA device enforcement)
Reported Feb 18, 2015
MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Craniomaxillofacial Division
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 11, 2015
Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health
FDA (openFDA device enforcement)
Reported Feb 10, 2015
Whole Foods Markets, Inc. Retira Productos Debido A Un Posible Error De Rotulacin Y A Un Alrgeno No Declarado
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
GE Healthcare, Proteus XR/a with wall stand model number 600-0301.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
lnline Persuader- PedFuse Pedicle Screw System; Part Number: 11-80164
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SpineFrontier, Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2015
CSA Medical truFreeze System; Model: CC3-01, a cryogenic surgical device ***The involved units are those with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CSA Medical
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Harmony¿ vLED Surgical Lighting System, one unit packaged per box The Harmony¿ vLED Surgical Lighting System is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Citizen Chef Organic Superfood Salad- 4 Organic Salads. Power Greens, Walnuts, Feta, Dried Cranberries and Blueberries…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taylor Farms Pacific Inc. (MacArthur Facility)
FDA (openFDA food enforcement)
Reported Dec 31, 2014
Maquet Quadrox-ID Pediatric Diffusion Membrane Oxygenator with Bioline Coating; Part Number BEQ-HMOD-30000 For cardiac…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Dec 31, 2014
North Carolina Firm Recalls Canned Soup Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.North Carolina Firm
USDA FSIS
Reported Dec 24, 2014
ASTS-LG1212: Anterior Lumbar Interbody Fusion Spine Truss System (orthopedic implant) Large, 12 degrees lordosis, 12 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.4-Web Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2014
AMS Monarc + Subfascial Hammock with Tensioning Suture REF 72404193 and AMS Monarc C Subfascial Hammock with Tensioning…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Medical Systems, Inc.
1 more product in this recall
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.