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 Mar 11, 2020
Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seca
FDA (openFDA device enforcement)
Reported Mar 4, 2020
Selenia Dimensions Mammography System, Model number ASY-04160, Selenia Dimensions Gantry, UDI 15420045505636,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2020
SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
The Bard Intra-abdominal Pressure Monitoring Device is composed of a tubing set used for infusing fluid into the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2020
Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Almark Foods, LLC
28 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Garlic Parmesan Sauce; DP# 4478 FG# 02620 8/16 fl. oz (4.73 ml) pouches; NET WT. 8.05 lbs (3.65 kg) Produced for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Golden State Foods
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 12, 2020
Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Bard Conquest 40 PTA Dilation Catheter, 8mm X 20mm x 75cm (CQF7582), 8mm x 40mm x 75cm (CQF7584); Recommended Guidewire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
CS5/5+ Fastpacks, 225 mL, 150¿ Res Autotransfusion Device - Product Usage: its related accessory components are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haemonetics Corporation
21 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Jeni's Dairy Free Cold Brew with Coconut Cream Pints frozen dessert
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jeni's Splendid Ice Creams LLC
FDA (openFDA food enforcement)
Reported Feb 5, 2020
Healon GV PRO 0.85 mL, Model (U.S.): 10-2400-14, Model (O.U.S.): 10-2705-14, 10-2715-14, 10-2725-14, and 10-2755-14
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2020
Dimercaptopropanesulfonate Sodium (DMPS), Aqueous injection solution, 50mg/mL 5 mL SDV, Rx only, McGuff Compounding…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McGuff Compounding Pharmacy Services, Inc.
FDA (openFDA drug enforcement)
Reported Feb 5, 2020
RayStation stand-alone software treatment planning system. Models 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jan 29, 2020
Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paltop Advanced Dental Solutions Ltd.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
ADVANCED ENDOSEE System CANNULA, Cooper Surgical Product Code/Model Number: ESPX5 The Advanced Endosee Cannula…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
Microbiologics QC Sets and Panels, Gram-Positive Blood Culture Control Panel (Inactivated Pellet), Catalog # 8180 Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2020
Cios Alpha, Model Number 10308191; mobile X-Ray system designed to provide X-ray imaging of the anatomical structures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2020
GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G), UPC 8 53152 00308 1 , 4 OZ (113 G) UPC 8 53152…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TFI Holding dba Grey Ghost Bakery
FDA (openFDA food enforcement)
Reported Jan 8, 2020
i-STAT cTnI cartridge
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
HeartMate 3 Mobile Power Unit, REF 107754, UDI or GTIN: 00813024010883, and 107758, UDI or GTIN: 00813024010890, when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Corp.
FDA (openFDA device enforcement)
Reported Jan 8, 2020
Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
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.