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 Feb 26, 2014
Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt system is intended to shut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap, Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2014
Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine HCl Injection, USP, 10 mg/mL, Lot 25-090-DK.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2014
Superstand stand-up wheelchair HPS-2 A standup wheelchair is a device with wheels that is intended for medical purposes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Standing Company
FDA (openFDA device enforcement)
Reported Feb 19, 2014
enGen Track System with enGen Select v5.0 with autoverification enabled Product The VITROS 5,1 FS Chemistry System with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 12, 2014
XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radiation therapy or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 12, 2014
GE Healthcare Precision 500D, Precision MPI & Precision RXI X-ray imaging systems. The Precision 500D R&F X-ray System…
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 Feb 12, 2014
Medtronic Advanced Energy Aquamantys3 Pump Generator; Product Catalog Number: 10-1357 (Generator assembly), 40-404-1(as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Advanced Energy, LLC
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Kimberly-Clark RadiOpaque Radiofrequency Cannula, Gauge 22, Length 100 mm, Active Tip 10 mm, Distributed in the US by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
FDA (openFDA device enforcement)
Reported Jan 29, 2014
AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Churchill Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 29, 2014
VITROS Chemistry Products COCM Reagent
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Leica BIOSYSTEMS; BOND Polymer Refine Red Detection; Catalog No: DS9390; Leica Biosystems Newcastle Ltd; Balliol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Newcastle Ltd.
FDA (openFDA device enforcement)
Reported Jan 8, 2014
VERIFY¿ Dual Species Self-Contained Biological Indicator, Distributed by STERIS Corporation, Mentor, OH. Intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2014
Stuffed Foods Asiago Risotto Bites; UPC 850821-00301
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stuffed Foods LLC
FDA (openFDA food enforcement)
Reported Jan 1, 2014
Macaroni Reg CAD, Formula MA.50, Macaroni Salad, packaged: -7-Eleven Fresh to Go Macaroni Salad, 12/7-oz carton cases.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc.
212 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2014
Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm Imaging Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2013
Chocolate Cream Pie, 4.5 oz. package, 12 pks/case. UPC # 891796002732
High riskUsing this product could cause serious injury, illness or death — stop using it now.3 Fellers
FDA (openFDA food enforcement)
Reported Dec 25, 2013
Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion Pumps are designed for use in care areas for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2013
AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile, wheeled transportation unit utilized to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Dec 11, 2013
Easy Diagnost Eleva Universal Fluoroscopic applications
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2013
GE Healthcare Discovery NMCT 670, Discovery NM 630, Optima NMCT 640, & Brivo NM 615. The GE Discovery NMJCT 670 system…
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 Nov 27, 2013
The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Vascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
VITROS Chemistry Products ACET Slides, 90 slides/pack; catalog number 1037274 VITROS Chemistry Products ACET Slides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
36 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
Sterrad 100NX, Product Code: 10104. Used to sterilize heat and moisture sensitive reusable medical devices.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
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.