All recall categories

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.

Medical devices

Reported Nov 9, 2022

Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP 120803FP 120404FP 120804FP 120805FP 120806FP…

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

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 2, 2022

Vortex MP Port Titanium Low Profile Implanted Port with 5F attached Silicone Catheter and Tray. Indicated for central…

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

Angiodynamics, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 2, 2022

THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles UPC 7 93611 81925 2 REGRIGERATE AFTER OPENING. USE WITHIN 14…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

The Chai Box

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 2, 2022

GORE CARDIOFORM ASD Occluder. cardiovascular implant.

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

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 26, 2022

Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR, MitraClip G4 Clip Delivery System NT US/CDS0701-NT,…

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

Abbott Vascular

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 26, 2022

Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 00817 4 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP,…

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

Flowers Foods (Corporate Offices)

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"

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

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food enforcement)

Food

Reported Oct 26, 2022

Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product…

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

Seeking Health LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 12, 2022

Philips Respironics Amara View Minimal Contact Full-Face Mask

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

Philips Respironics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 5, 2022

"A&W Root Beer Zero Sugar" packaged in 20oz PET bottles. UPC: 00-0-78000-05340-1

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

Beverage Distribution Center Incorporated, LLC. (BDCI)

FDA (openFDA food enforcement)

Medical devices

Reported Oct 5, 2022

Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnostic images.

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

DICOM Grid, Inc. d/b/a Ambra Health

FDA (openFDA device enforcement)

Food

Reported Oct 5, 2022

Aged raw milk cheese "Ploughman Cider Wash Tomme" batch 47 4 oz to 12 oz packages

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

Keswick Creamery at Carrock Farms LLC

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 5, 2022

MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…

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

MEDLINE INDUSTRIES, LP - Northfield

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim…

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

Tandem Diabetes Care Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 28, 2022

AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse osmosis unit intended for use with hemodialysis systems.…

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

Fresenius Medical Care Holdings, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…

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

ICU Medical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

QIAcube Connect MDx, Model No. 9003070

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Food

Reported Sep 7, 2022

Wegmans Lemon Dill Finishing Butter, NET WT 3.5 OZ (99g), black plastic cup with a sealed lidding film under the lid.…

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

Epicurean Butter Co.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 7, 2022

T-SPOT.TB REF TB.300 US

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

Oxford Immunotec Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…

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

Medtronic Neuromodulation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 24, 2022

Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Tomato paste,…

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

Albertsons Companies LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 17, 2022

cobas e801 Immunoassay Analyzer

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10

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

Aesculap Implant Systems LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 10, 2022

UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool

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

Neotract Inc.

FDA (openFDA device enforcement)

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Other states

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.