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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.

1,477 stored notices name District of Columbia, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach District of Columbia too — those are in the archive.

Food

Reported Dec 4, 2024

Atwater's Spider Web Tarts, 26 tarts packaged individually, 5.73 in x 5.95 in x 3 in clear plastic clamshell container,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

One Roof LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 27, 2024

OrganOx metra -Intended as a Normothermic Machine Perfusion system of donor transport livers. Model/Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

OrganOx Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2024

Irrigation Tubing for KARL STORZ Endomat Select UP210 REF 031523-10 Tubing Set, Irrigation, PC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

Abbott Alinity m HPV AMP Kit, used with the Alinity m System, product codes: a) REF 09N15-095; b) REF 09N15-090; c) REF…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Molecular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

1) Flex Extenders, 5.2" x 15mm OD x 15mm ID REF S6411P 2) Flex Extender, 5.2" x 15mm OD x 22/15mm ID REF 7 5132 The…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Westmed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing Levels 1 & 2 6 X 15 mL-IVD intended as a…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mckesson Medical-Surgical Inc. Corporate Office

FDA (openFDA device enforcement)

Food

Reported Oct 23, 2024

S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranford, NJ, 07016

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Nuts.com

FDA (openFDA food enforcement)

Food

Reported Oct 23, 2024

Grabeez The Big Cheese SNACK MIX Net Wt. 3.25 oz (92g) Ingredients: Peanuts***Cheese Pretzel Gems***Vegetable…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tropical Nut & Fruit Company

FDA (openFDA food enforcement)

Medical devices

Reported Oct 16, 2024

Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. Monarch Platform (Bronchoscopy), REF: MON-000006,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Auris Health Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2024

MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing W/APPLICATOR, 1.5oz tube (Model Number 31515)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2024

DAILIES TOTAL1, DAILIES TOTAL1 for Astigmatism, DAILIES TOTAL1 Multifocal, TOTAL30 Sphere,

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 9, 2024

MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 700G Insulin Pump, REF:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medtronic MiniMed, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2024

PT301US Airvo 3 Respiratory Support Device with software version 1.2.0 and/or 1.5.1 The Airvo 3 is intended to provide…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fisher & Paykel Healthcare, Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2024

Karl Storz - Endoskope , REF: 27092AMA, Hopkins Telescope 6, Rx only, CE 0123

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Karl Storz Endoscopy

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2024

Alaris System PC Unit Model 8015 - a modular infusion pump and monitoring system

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

CareFusion 303, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 25, 2024

Wegmans PECAN BLEND NET WT 16OZ (1LB) 453g Ingredients: Pecans, Cashews, Pistachios, Canola and/or Peanut and/or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Flagstone Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 25, 2024

ViewPoint; system, imaging processing, radiological

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare GmbH

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2024

HAWK Warming Grid, Item Number: 59-300

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Safeguard US Operating LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2024

American Outdoor Products - Astronaut Strawberries, packaged in 0.5oz (14g) metallic plastic pouches. Sold individually…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

American Outdoor Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2024

FILMARRAY 2.0 INSTRUMENT, REF: FLM2-ASY-0001, FLM2-ASY-0001-W

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)

Food

Reported Sep 18, 2024

BDAY CAKE MOCHI CRUNCH packed in pink plastic pouch packaging, net wt. 5oz, UPC 7189147148, Orwaiian LLC, 465 NE…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Orwaiian LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 11, 2024

Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

W L Gore & Associates, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2024

McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Covidien

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2024

ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Inari Medical - Oak Canyon

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.