Recalls distributed in Delaware
These notices name Delaware 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.
1,697 stored notices name Delaware, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Delaware too — those are in the archive.
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)
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)
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)
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)
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)
Reported Sep 18, 2024
IBA Proton Therapy System - PROTEUS 235 ProteusPLUS and ProteusONE Software versions: PTS-8 versions, PTS-10 versions,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Brand Name: Vit-l-escence Product Name: Vit-l-escence Singles A3 Model/Catalog Number: 1203- Software Version: N/A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ultradent Products, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2024
Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo, O2, Benelux EV300; BR2200X18B Trilogy…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
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)
Reported Sep 4, 2024
DR 800. Digital Radiography X-ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Agfa N.V.
FDA (openFDA device enforcement)
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)
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)
Reported Aug 28, 2024
Great Value; 8oz Apple Juice in 6 pack; 100% Juice; packaged in 8 oz. PET plastic bottles; UPC 0-78742-29655-5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Refresco Beverages US Inc.
FDA (openFDA food enforcement)
Reported Aug 28, 2024
Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2024
WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Aug 21, 2024
Cepheid, Sample Collection Device, Part: 900-0370
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cepheid
FDA (openFDA device enforcement)
Reported Aug 21, 2024
Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Rapid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
22 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 21, 2024
Fox's u-bet Sugar-Free Chocolate Flavored Syrup, 18oz, UPC 070216246004, 12 retail units per wholesale case
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Subco Foods Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 21, 2024
HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
FDA (openFDA device enforcement)
Reported Aug 14, 2024
BIOFIRE FILMARRAY Gastrointestinal (GI) Panel REF RFIT-ASY-0116 (30 test kit) BIOFIRE FILMARRAY Gastrointestinal (GI)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Aug 14, 2024
TruDi NAV Suction, 0 Degrees; Model/Catalog Number: TDNS000Z. TruDi" NAV Suction Instruments are intended for use with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Aug 14, 2024
Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Aug 14, 2024
Medline procedure kits labeled as: 1) CONTINUOUS BLOCK, Pack Number DYNJRA0960C; 2) COMBINED SPINAL AND EPIDURAL, Pack…
High riskUsing this product could cause serious injury, illness or death — stop using it now.MEDLINE INDUSTRIES, LP - Northfield
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 14, 2024
Nuts.com Ground Sumac 1 lb resealable stand-up pouches and 20 lb double lined plastic bags in a cardboard box.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nuts.com
FDA (openFDA food enforcement)
Free recall alerts
Get alerted about new Delaware recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.