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 May 4, 2016
GE Healthcare, Aisys and Aisys CS2. Intended to provide general inhalation anesthesia and ventilator support to a wide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Acorn 180 Curved Stairlift
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acorn Stairlifts Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Boston Scientific Fetch 2 Aspiration Catheter, Catalog No. 109400-001. Product The Fetch 2 Aspiration Catheter is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Apr 27, 2016
OraQuick HCV Visual Reference Panel Intended to assist new operation in becoming proficient at reading specimens with…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.OraSure Technologies, Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
Siemens SOMATOM Definition: Intended to produce cross-sectional images of the body. Computed tomography (CT) x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
BD-Retic-Count Reticulocyte Reagent System; Hematology: Used for in vitro diagnostics
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Apr 20, 2016
GE Healthcare, Aisys CS2 anesthesia..
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Diana Automated Compounding System, Diana Onco Plus, Item No. ASN220 The Diana is an automated compounding device for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
Brilliance 64:Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2016
X-Guide Surgical Navigation System, X-Clip Bulk Kit The X-Guide Surgical Navigation System is a computerized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.X-NAV Technologies, LLC
FDA (openFDA device enforcement)
Reported Apr 13, 2016
Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute and Chronic Hemodialysis
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 13, 2016
GE Inspection Technologies, LP, Cabinet X-ray system used for industrial quality control.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Inspection Technologies, LP
FDA (openFDA device enforcement)
Reported Apr 13, 2016
The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog CLXUSA. Manufacturing lot D342 UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Therakos Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Reveal LINQ insertable Cardiac Monitor, Model LNQ11. Monitors subcutaneous ECG continuously.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the…
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 30, 2016
Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC, Size 3 - Catalog # AR-503-TTTD, Size 4 -Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Chappaqua Crunch Simply Granola with Blueberries & Bananas, in 13 ounce clear plastic pouch. UPC:7 86516 16007 9
High riskUsing this product could cause serious injury, illness or death — stop using it now.D.S. Waugh
FDA (openFDA food enforcement)
Reported Mar 23, 2016
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom) Powered stretcher
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Large Volume Paracentesis Kit is packaged in a thermaformed tray which contains slots and snap-in holders for most…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gi Supply
FDA (openFDA device enforcement)
Reported Mar 9, 2016
BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2016
BD FMC7 FITC: Model 430918. FMC7 is intended for in vitro diagnostic use in the identification of cells expressing FMC7…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Becton, Dickinson and Company, BD Biosciences
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.