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.
Reported Jul 1, 2020
Atellica Solution IM1300 Analyzer, Siemens Material Number 11066001, UDI # 00630414007960
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2020
PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: The Biosense Webster…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2020
Leica ARveo and M530 OH6 microscope systems.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2020
VITROS Chemistry Product AMYL Slides Reagent, AMYLASE/5 PACK/300 SLDS, Product Code 1202670, UDI # 10758750008513 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Bin Butternut Squash, Bulk, Raw Product in Bins / 4, 5lb packages in each case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coastal Sunbelt Produce Co. Inc.
FDA (openFDA food enforcement)
Reported Jun 17, 2020
Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Endologix, Inc.
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Triever20 Aspiration Guide Catheter a component of FlowTriever Retrieval/ Aspiration System, UDI: 00850291007079
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inari Medical
FDA (openFDA device enforcement)
Reported Jun 17, 2020
Infant/Child Reduced Energy Defibrillation Electrodes, Part Number: 3202380-006, for use with LIFEPAK 1000…
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 Jun 17, 2020
RayStation 4.0 to RayStation 5 Service Pack 2 - Product Usage: For radiation therapy and medical oncology which can…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
14 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 17, 2020
ADVIA Chemistry Fructosamine Reagent (FRUC), Siemens Material Number 10361941, UDI Number 00630414558073 - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Gambro Cartridge Blood Set Prime Line - Product Usage: is intended for single use in a hemodialysis treatment using…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Beckman Coulter Access Immunoassay Systems, Access Free T4 Thyroxine, REF 33880 (UDI:15099590225834) for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
Pressure Monitoring Set, C-PMS, G02838
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
System, Tomography Computed Emmission
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 10, 2020
OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Osteomed, LLC
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2020
CooperSurgical Dilator/Sound Set, Rx only, Sterile/EO, Made in South Korea, P/N MX21
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2020
GENTLEWAVE REF: FG-002-0001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonendo Inc.
FDA (openFDA device enforcement)
Reported May 20, 2020
Joseph's Gluten Free Original Wrap, 4 wraps, Net. Wt. 5.6 oz., UPC Code: 074117-003612
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Middle East Bakery, Inc.
FDA (openFDA food enforcement)
Reported May 13, 2020
da Vinci Xi Surgical System, IS4000 - Product Usage: The da Vinci Xi surgical system (IS4000) is made of three main…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2020
Visualase Cooled Laser Applicator System Tubing Set kits Product numbers: VCLAS 9735559, 3mm tip/1.65mm catheter VCLAS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported May 13, 2020
NUVASIVE MAGEC 2 Rod X.X mm XX mm, REF MC2-XXXXS LOT 0000000 AAA - Product Usage: comprised of a sterile single-use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Inc.
FDA (openFDA device enforcement)
Reported May 13, 2020
Varian Multileaf Collimator [MLC]; Millenium Multileaf Collimator [52, 80, 120 leaf]; High Definition 120 Multileaf…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
CapsoCAM Plus, UDI: 00867770000209
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Capso Vision, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2020
PreludeSYNC DISTAL Radial Compression Devices, SDRB-REG-LT, SDRB-REG-RT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
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.