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.
1,478 stored notices name District of Columbia, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach District of Columbia too — those are in the archive.
Reported Jul 21, 2021
Lingen Disposable Virus Sampling Kit, Item MTM-04, 40 tubes/box.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mercedes Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Heart Valves Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 14, 2021
FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems, Kappa Freie Leichtkette (Human) kit for Roche cobas…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Binding Site Group, Ltd.
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 7, 2021
Lyra SARS-CoV-2 Assay (M120) in vitro diagnostic test reagent
High riskUsing this product could cause serious injury, illness or death — stop using it now.Quidel Corporation
FDA (openFDA device enforcement)
Reported Jun 30, 2021
inLight Medical LED Pads used with Polychromatic light technology system
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Inlightened Partners LLC
FDA (openFDA device enforcement)
Reported Jun 23, 2021
The Better-Bladder (BB), part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass circuits. Model: BB14
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Circulatory Technology Inc.
FDA (openFDA device enforcement)
Reported Jun 23, 2021
Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer Medical ApS
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
COVID-19 Self-Test Kit *** INNOVA *** 7T
High riskUsing this product could cause serious injury, illness or death — stop using it now.Innova Medical Group, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 16, 2021
Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Normand-Info S.A.S.U.
FDA (openFDA device enforcement)
Reported Jun 16, 2021
RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 ,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 2, 2021
IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported May 26, 2021
PUBLIC GOODS brand HAIR, SKIN, & NAILS Dietary Supplement; 60 tablets per bottle; Other ingredients: Stearic acid;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Public Goods
FDA (openFDA food enforcement)
Reported May 26, 2021
Alpha Interlock Suspension System Lanyard Body: An external prosthetic device. The Alpha Lanyard includes suction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WillowWood Global LLC
FDA (openFDA device enforcement)
Reported May 19, 2021
REF CH3397 Oncology Kit w/Spiros¿, Red Cap, Bag Spike w/Clave Additive Port LOT 5118610 - Product Usage: for use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
25 more products in this recall
FDA (openFDA device enforcement)
Reported May 19, 2021
Calibration Serum Level 3 (CAL 3) - multi-analyte mixture calibrator. Catalogue Number: CAL2351
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Randox Laboratories Ltd.
FDA (openFDA device enforcement)
Reported May 19, 2021
ASSURITY Pulse Generator REF PM**** SN ********* ST. JUDE MEDICAL Assurity and Endurity pacemakers are intended to…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St. Jude Medical, Cardian Rhythm Management Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 12, 2021
Grace Medical REF S-2500 *** SHEEHY BONE DUST COLLECTOR *** Stainless steel filter - Product Usage: intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oto Med Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 28, 2021
Trader Joe's Restaurant Style White Corn Tortilla Chips; Net Wt. 9 oz. (255g)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snak King Corporation
FDA (openFDA food enforcement)
Reported Apr 21, 2021
Prodisc C - prosthesis, intervertebral disc - Product Usage: indicated in skeletally mature patients for reconstruction…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Centinel Spine, Inc.
FDA (openFDA device enforcement)
Reported Apr 21, 2021
HARRIS TEETER FRESH FOODS MARKET 3 Layer COOKIES & CREME CAKE NET WT 48 OZ (3 LB) 1.36kg packages PROUDLY DISTRIBUTED…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Harris Teeter
FDA (openFDA food enforcement)
Reported Apr 14, 2021
Enteral Infusion Pump
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
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.