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 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, 2016
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)
Reported Dec 2, 2015
Skippy Creamy 25% Less Fat Reduced Fat Peanut Butter Spread Net Wt. 16.3 OZ (1 lb 0.3 OZ) 462g in plastic jars, UPC:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hormel Foods Corporation
FDA (openFDA food enforcement)
Reported Dec 2, 2015
Dimension Vista System (MG) ; Flex reagent cartridge Catalog number K3057, SMN 10445158. For the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2015
MiniArc Pro Single incision Sling System, Model number / Product Reference 9000261, Lot 936405xxx. Designed to treat…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Astora
FDA (openFDA device enforcement)
Reported Nov 18, 2015
RotaWire Elite and wireClip Torquer, Guidewire and Guidewire Manipulation Device, Floppy. REF H802223301 (5-pack outer…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Stryker Orthopaedics, MIS MODULAR DISTAL CAPTURE TRIATHLON MIS INSTRUMENTS, REF 6541-5-723, Lot AdminECR19205,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 18, 2015
Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WalkMed Infusion, LLC
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.