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 Mar 9, 2016
Medtronic Custom Perfusion Tubing Pack, Rx, Sterile EO. Terumo Cardiovascular Systems (Terumo CVS) has distributed an…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Mar 9, 2016
BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2016
This reagent is for in vitro diagnostic use. Pax-5 (1EW) monoclonal antibody is intended to be used for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2016
software for Syngo Dynamics a Picture Archiving and Communication System (PACS) intended for acceptance, transfer,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet France SARL
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic surgical instrument used in hip arthroscopy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Feb 10, 2016
ACIST Medical Systems, BT2000 Automated Manifold Kit (SKU 014613) and CPT2000 (SKU 014623) Automated Manifold Kits,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acist Medical Systems
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by Mars Chocolate na, llc Hackettstown, NJ…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mars Chocolate North America
FDA (openFDA food enforcement)
Reported Feb 10, 2016
Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Resmed Corporation
FDA (openFDA device enforcement)
Reported Feb 3, 2016
Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Midmark Corp. dba Progeny Inc.
FDA (openFDA device enforcement)
Reported Jan 27, 2016
FMS neXtra¿ 3.5mm Full Radius Cutter Shaver Blades; Product Code: 283305 Intended to provide controlled cutting,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2016Updated Oct 23, 2026
Berks Packing Co. Recalls Beef Products Due to Misbranding
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Berks Packing Co., Inc.
USDA FSIS
Reported Jan 20, 2016
UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response 5.5/6.0 Spine System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skytron, Div. The KMW Group, Inc.
FDA (openFDA device enforcement)
Reported Jan 6, 2016
MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jan 6, 2016
Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Vancomycin Screen Agar
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2015
A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Dec 30, 2015
Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 23, 2015
MOSAIQ Oncology Information System. Used to manage workflows for treatment planning and delivery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Dec 16, 2015
Red Bull Total Zero Energy Drink, 12 fl.oz. (355ml), UPC CODE(S): ON THE CAN: 6 11269 62373 4; ON THE CASE: 6 11269…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Red Bull North America Inc.
FDA (openFDA food enforcement)
Reported Dec 2, 2015
Natures Promise Organic Shelled Edamame, 16 oz., UPC 68826712764. Product is frozen.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Green Organic Vegetables Incorporated
1 more product in this recall
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.