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.
1,727 stored notices name Delaware, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Delaware too — those are in the archive.
Reported Sep 11, 2013
Chocolate covered raisinsin 4 oz flexible bags labeled in part "***Pennsylvania Dutch Candies***Chocolate Covered…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Warrell Corporation
FDA (openFDA food enforcement)
Reported Sep 4, 2013
HSV 2 Primers, Catalog #18081020. Analyte Specific Reagent. The HSV-2 primer pair is specific for HSV-2 (Herpes Simplex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Philips Easy Upgrade DR, Code No: 712086 This system is used for making X-Ray exposures for diagnostics.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Synthes 2.4mm VA-LCP Two Column Volar Distal Radius Plate and Torque limiting attachment, 1.2Nm Synthes VA-LCP Distal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Aug 21, 2013
1) Adult Manual Resuscitator, 2K8004, Oxygen Reservoir Bag, Adult Mask; 2) Adult Manual Resuscitator, 2K8005, 40" (1.0…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported Aug 21, 2013
Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375, 2) 6801890, 3) 6802445, 4) 6802413 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Vena Cava Filter and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cordis Corporation
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Medtronic Mullins Transseptal Adult 7F, REF 008551. Intended for the introduction of cardiovascular catheters into the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
FDA (openFDA device enforcement)
Reported Aug 14, 2013
Earth's Pride Organics: Organic Oregano, 2.2 oz. Packaged at 12 units per case. Packaged in a glass jar with cork…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olde Thompson, Inc.
FDA (openFDA food enforcement)
Reported Aug 14, 2013
TCM4 series Base Units, and spare part Power Supply, Radiometer Medical ApS, Akandevej 21, Br¿nsh¿j, Denmark,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Aug 14, 2013
ADVIA Centaur Systems TSH3 Ultra ReadyPack ((REF 06491072 - 100 Tests, REF 06491080 - 500 Tests, REF 04862625 - 2500T).…
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 Aug 14, 2013
Raw Pistachio Halves, 1 pound bag. Item Number 11910, UPC Code: 172043119107; Raw Pistachio Halves, 4 pound bag. Item…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Superior Nut Co. Inc.
FDA (openFDA food enforcement)
Reported Aug 7, 2013
GE Healthcare, VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM. The device is a general purpose ultrasound…
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 Aug 7, 2013
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Picis Inc.
FDA (openFDA device enforcement)
Reported Aug 7, 2013
AIA Analyzer Pipette Tips used on Tosoh AIA-2000, AIA-1800, AIA-900 and AIA-600II Analyzers, 1000 tips/bag AIA-Analyzer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Smd Inc.
FDA (openFDA device enforcement)
Reported Jul 31, 2013
Magnesium Sulfate 2 grams in Dextrose 5% for Injection, in 50 mL Plastic Infusion Bags, Med Prep Consulting Inc.,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Med Prep Consulting, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jul 24, 2013
Synthes CMF Distraction System The product is intended for use as a bone stabilizer and lengthening (and/or transport)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2013
CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules and Hematocrit/Saturation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2013
RigiflexTM 11 Single-Use Achalasia Balloon Dilator, Material Number (UPN) M00554510 Product Usage: The Boston…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Boston Scientific Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2013
Fudge Buttercream Frosted Peanut Butter cookies, some of which were mislabeled by being wrapped in Buttercream Frosted…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cheryls
FDA (openFDA food enforcement)
Reported Jul 10, 2013
Computed Tomography X-ray systems Product Usage: The Brilliance CT 64, Ingenuity Core, and Ingenuity Core128 scanners…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) 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.