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 Feb 1, 2023
Wegmans Organic Farm & Orchard Micro Greens; 1.75 oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2023
VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2023
Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2022
The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Dec 28, 2022
King Oscar Anchovies Flat Fillet in Olive Oil 2 oz. can 18 cans per carton UPC number: 3480060061 Ingredients:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tri-Union Frozen Products Inc.
FDA (openFDA food enforcement)
Reported Dec 21, 2022
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
FDA (openFDA device enforcement)
Reported Dec 14, 2022
LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Implants Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 14, 2022
Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nestle-USA, Inc. (Corporate Office)
FDA (openFDA food enforcement)
Reported Dec 7, 2022
Accelerate PhenoTest BC kit REF 10101018
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accelerate Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 7, 2022
CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200; BM-AD4K0200 BM-ADK0200 BM-CDK0200 BM-CFDK0200…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GS Biomark LLC
FDA (openFDA device enforcement)
Reported Nov 23, 2022
Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 23, 2022
Visualase Cooled Laser Applicator System (VCLAS) 9735560 .4MM CORE FIBER 10MM TIP product. Used to necrotize or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2022
NaturaLyte Liquid Acid concentrate, Part Number 08-0231-4, four (4) one-gallon bottles per bottle case. For dialysis.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Hammond's Salted Caramel Cookies, NET WT. 5 OZ (142g), UPC 6 91355 89889 5, Manufactured for: Hammond's Candies, 5735…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hammond's Candies Since 1920 II, LLC
FDA (openFDA food enforcement)
Reported Nov 16, 2022
Zio AT Clinical Reference Manual, Part: ALB0031, and Zio AT Important Information Pamphlet, Part: ALB0034. For Zio…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iRhythm Technologies, Inc.
FDA (openFDA device enforcement)
Reported Nov 16, 2022
Insulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 9, 2022
BD Trucount Tubes (Cat. No. 340334), used for determining absolute counts of leucocytes in blood. BD Trucount tubes are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
2 more products in this recall
FDA (openFDA device enforcement)
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)
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)
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)
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)
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)
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)
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)
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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.