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 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)
Reported Dec 14, 2016
Xcela Power Injectable PICC Maximal Barrier Nursing Kit The Maximal Barrier Nursing Kits are Tandem Pack Convenience…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics Inc. (Navilyst Medical Inc.)
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Model 37751 Recharger Product Usage: The Medtronic 37751 Recharger is a hand-held device used to charge the battery in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Dec 14, 2016
Merge, eFilm Workstation and eFilm Lite eFilm Workstation with Modules is a software application that is used for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2016
MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for tissue release of the transverse carpal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thayer Intellectual Property, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Koffee Kup Potatoe Hamburger Buns, Plain and Seeded, 8 pk
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Koffee Kup Bakery Inc.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 16, 2016
Accessory Adapter Part number 600525A0 Product Usage: designed for the mounting of MAQUET accessories with the dovetail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Select Recipe Buttermilk Ranch Dressing, Net contents: 1 GAL (3.79 L), 4 X 1 GAL
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Oasis Foods Co.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 2, 2016
ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US, ex-tem. Used to monitor the coagulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TEM Systems Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Awareness Corporation
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Endoscopic Articulating Linear Cutter, ATB35. Standard 35 MM. The ENDOPATH ETS-Flex Endoscopic Articulating Linear…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
HeartWare Ventricular Assist System Controller Product Usage: For use as a bridge-to-cardiac transplantation in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Oct 26, 2016
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Oct 19, 2016
HeartWare Ventricular Assist System (HVAD), US product: Model No.: 1103; and International Product: Model No.: 1104XX.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare, Inc.
FDA (openFDA device enforcement)
Reported Oct 12, 2016
Thermo Scientific QMS Everolimus Assay; Model number: 0380000 (US Distribution); 0373852 (Foreign Distribution) Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corporation
FDA (openFDA device enforcement)
Reported Oct 5, 2016
The EKOS cart has the catalog number 700-60101. The EKOS cart is a custom infusion stand/cart used to hold and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.EKOS Corporation
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.