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 Jun 17, 2015
MX 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
34 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2015
Oncentra Brachy radiation therapy planning software designed to analyze and plan radiation treatments in three…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
D-fend, (p/n 876446-HEL), and D-fend+ (p/n 881319-HEL) water trap. Used with Compact Airway Modules E/M-C(Ai)O(V)(X)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Jun 3, 2015
Medtronic SynchroMed II Implantable Infusion Pumps, models 8637-20 and 8637-40. Sterile. Product Usage: The implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Jun 3, 2015
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 27, 2015
Black & White Mini Cookies, Net Wt. 2 oz. (56 g), SKU 408785, UPC code 833282000495, Manufactured for: Starbucks Coffee…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sweet Sam's Baking Company, LLC
FDA (openFDA food enforcement)
Reported May 20, 2015
Nuclear Gamma Cameras (ADAC Vertex Classic, ADAC VERTEX PLUS/SOLUS/CARDIO, ADAC VERTEX V60) Philips Medical Systems,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 20, 2015
Poco Dolce Bittersweet Chocolate: Burnt Caramel Tile, sea salt topped; 0.6 oz (17 grams) San Francisco CA. Ingredients:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Poco Dolce Confections, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 20, 2015
Trader Joe's Nuts Raw California Walnut Pieces NET WT. 16oz. (1 LB) 454g UPC 00373685 Trader Joe's Nuts Raw California…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Trader Joes Company
FDA (openFDA food enforcement)
Reported May 20, 2015
Guacamole Dip Net Wt. 8 OZ. (.5LB) Distributed By: Whole Foods Market UPC/PLU: 0-36406-30279-0; WFM Dip Guacamole PPK…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market
38 more products in this recall
FDA (openFDA food enforcement)
Reported May 13, 2015
BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g x 20cm The BARD MAX-CORE Disposable Core Biopsy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported May 13, 2015
EPIQ 5 Ultrasound System with Pediatric Cardiology option, Model: EPIQ 5G, EPIC 5C, EPIQ 5W. Catalog Number: 795204 /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 6, 2015
Caviwave Pro Ultrasonic Cleaning System, Product Usage: To wash (remove tissue, blood and other contaminants) or dry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 6, 2015
Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 for orthopedic surgery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2015
The PCA 3 infusion pump allows clinicians, or patients, to (self) Administer analgesia safely and effectively within…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2015
WALLACH LL 100 cryosurgical units: LL100 Cryosurgical - Part Number 900001; LL110 with Pinned Yoke - Part Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Apr 22, 2015
Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2015
CS 8100, CATALOG # (s): 5303045, 5311129, 5303060, 5303110 Intended to produce complete or segmented tomographic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carestream Health, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 15, 2015
VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number VPS-G4C Cardiovascular: The VPS Stylet and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VasoNova, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Cheryl's Buttercream Frosted Cut-Out BUNNY HEAD COOKIES, Net Wt 1.5oz (43g), Cheryl's Westerville, Ohio 43082…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cheryls
FDA (openFDA food enforcement)
Reported Apr 8, 2015
Honey & Oat Mixers ready-to-eat dry cereal sold under the market pantry brand and packaged in card stock cartons with a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gilster-Mary Lee Corp.
FDA (openFDA food enforcement)
Reported Apr 8, 2015
Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
LIS27T - Lacrimal Intubation Set RX Only Sterile Used in various ophthalmology procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quest Medical, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
GE Healthcare, SIGNA 1.5T TWINSPEED, SIGNA INFINITY MRISYSTEM, SIGNA 3.0T INFINITY WITH EXCITE, SIGNA 3.0T WITH EXCITE,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
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.