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 13, 2017
TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM), Catalog Number 221261 Trypticase Soy Agar with 5% or 10% Sheep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2017
Organic traditions brand DARK CHOCOLATE HAZELNUTS, NET WT. 3.5 oz (100 g) - UPC 8 54260 01400 6, and NET WT. 8 oz (227…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Health Matters America Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 13, 2017
Fit & Active Chocolatey Chip Protein Meal Bars; UPC: 41498 18695; Lot Code: Q209MY; Expiration date: May 24, 2018
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leclerc Foods USA
FDA (openFDA food enforcement)
Reported Nov 29, 2017
Dried Dark Chocolate Covered Cherries, The products are packaged in 25-pound corrugated boxes and 6 oz. and 24 oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shoreline Fruit, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 29, 2017
ROSA Brain 3.0 Intended for the spatial positioning and orientation of instrument holders or tool guides to be used by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 18, 2017
waterfront Bistro Tatar Sauce, Net Wt 9 oz. (255g), UPC 21130-12242
High riskUsing this product could cause serious injury, illness or death — stop using it now.Silver Spring Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 11, 2017
Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
FDA (openFDA device enforcement)
Reported Sep 27, 2017
Spine Referencing Instrumentation, Spinous Process Clamp, Tall When used with a Medtronic StealthStation Navigation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 13, 2017
MOSAIQ Medical Charged-Particle Radiation Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
Michele s Toasted Muesli, 16 oz bags, 12 units per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Michele's Granola LLC
FDA (openFDA food enforcement)
Reported Aug 30, 2017
DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Plum 360 Infusion System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2017
ROSA Brain, 3.0.0 The device is intended for the spatial positioning and orientation of instrument holders or tool…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Aug 2, 2017
STOCKERT Heater-Cooler System 3T, 230 V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Agfa Healthcare NX 3.0.8950 Imaging Processing Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oscor, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Nussloch GmbH ASP6025 Tissue Processor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Green Tea Ice Cream: Sold under the brand names of: Trader Joe's Brand Matcha- 1 quart tubs, SKU 055740; Shirakiku…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mikawaya
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Philips DigitalDiagnost 3.1.x X-Ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 14, 2017
STILL RIDING FOODS GLUTEN FREE PIZZA CRUST; Sold in the following package sizes: 36/9" NET WT 15lbs (6.80kg); 12/12"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Still Riding Foods, LLC
FDA (openFDA food 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.