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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.

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Food

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

Reported Oct 5, 2016

365 Everyday Value Mango Frozen Fruit Bars 4 Bars-4 fl. oz. (118 mL) each-Net 16 fl. oz. (472 mL) in a cardboard…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Whole Foods Market

FDA (openFDA food enforcement)

Food

Reported Sep 28, 2016

Cobblestone Bread Co. Wheat English Muffins, 12 oz. (6 count)plastic bag (340g) UPC: 0 72250 01316 1

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Flowers Foods

FDA (openFDA food enforcement)

Food

Reported Sep 28, 2016

ULTRA PROTEIN VANILLA¿ 948 grams, packaged in 2500cc White HDPE Canister

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hvl, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 28, 2016

O Organics Vegetable Tray, 18 oz. (1 lb. 2 oz.) 510g plastic tray. Best If Used By: AUG 11 UPC (incorrect, which is on…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Mann Packing Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 28, 2016

G1 Dissection Tool - 7mm FBALL L; For cutting and shaping bone including spine and cranium.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Anspach Effort, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2016

The VITROS¿ Chemistry Products Calibrator Kit 31, Lot 3155 used in conjunction with: VITROS¿ Chemistry Products HbA1c…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

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Other states

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.