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.
1,724 stored notices name Delaware, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Delaware too — those are in the archive.
Reported Aug 30, 2023
TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT, REF 71647336, Femur nail
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2023
Alpenfest Style Sachertote NET WT 17.6 OZ (1 LB 1.6OZ) 500g Frozen UPC:2010 0889 Packaged in Cardboard Carton.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lidl US TRADING
FDA (openFDA food enforcement)
Reported Aug 16, 2023
Caramel Butter Pecan Cup 14 fl oz. cup (8 per case) Paper cup with paper lid Brand: Eclipse Foods UPC: 810049270490…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eclipse Foods Co.
FDA (openFDA food enforcement)
Reported Aug 9, 2023
Outshine No Sugar Added Strawberry Fruit Bars Brand name: Outshine; Unit size:14.7 fl oz carton with 6 bars; Container…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dreyer's Grand Ice Cream, Inc.
FDA (openFDA food enforcement)
Reported Aug 9, 2023
OEC Flexiview 8800 Systems with 9-inch Image Intensifier
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2023
VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2023
NeuMoDx Cartridge-used for extraction, purification, amplification and detection of nucleic acids on the NeuMoDx 288…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuMoDx Molecular Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2023
Always-On Tip Tracked Instruments (SPiN Drive¿ instruments) Brush, 15mm L, 1.8mm OD Intended for use in clinical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
7 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
HAMILTON C1 Ventilator REF 161001 1610010 Is intended to provide positive pressure ventilatory support to adults and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 2, 2023
FRED Flow Re-Direction Endoluminal Device, REF: FRED3507-PMA, FRED3511, FRED3511-PMA, FRED3516-CA, FRED3516-PMA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microvention Inc.
FDA (openFDA device enforcement)
Reported Jul 26, 2023
Durepair Dura Regeneration Matrix: DUREPAIR DURA SUBSTITUTE 2 X 2, 61100; DUREPAIR DURA SUBSTITUTE 3 X 3, 61105;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Jul 12, 2023
BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2023
Cargill Trisodium Citrate Dihydrate packaged in 50 lb. paper bags and 2,000 lb. supersacks. Product item ids: 1. SKU…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cargill, Inc. Corporate Headquarters
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 12, 2023
da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 28, 2023
Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale [Model(s): RW82VHA-1, RW82VHA-1C, RW82VHA-1D,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 28, 2023
enterade Advanced Oncology Formula; Original Vanilla Flavor; Medical Food; Helps manage and maintain GI function; 8 FL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Entrinsic Health Solution Inc.
FDA (openFDA food enforcement)
Reported Jun 28, 2023
KARL STORZ Radel Sterilization Trays, Models: 27717A, 27717B, 39301A, 39301C, 39231XA, 39301C1, 39311A, 39317A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 28, 2023
Wegmans Italian Classics Diavolo Pasta Sauce 24 OZ
High riskUsing this product could cause serious injury, illness or death — stop using it now.LiDestri Foods, Inc.
FDA (openFDA food enforcement)
Reported Jun 28, 2023
Masimo RD Set TC-I SpO2 Adult Reusable Ear Sensor, REF: 4053
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Masimo Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Driver Instrument, part of the Superion Indirect Decompression System, REF: 102-9800, used with the Superion Indirect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Aspira Peritoneal Drainage Catheter Insertion Tray 15.5F, REF 4992206 Version A, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 21, 2023
Icelock 125 Ratchet, REF: L-125000; Icelock 600XM Ratchet, REF: L-621200; Icelock 621 Ratchet, REF: L-621000; Icelock…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
FDA (openFDA device enforcement)
Reported Jun 14, 2023
Tastykake Chocolate Kandy Kakes NET WT 8 OZ (227g) 6-1.3 OZ (38g) PKGS TASTY BAKING COMPANY, PHILADELPHIA, PA 19112 UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Flowers Foods (Corporate Offices)
FDA (openFDA food enforcement)
Reported Jun 14, 2023
Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12 8 fl. oz (236 mL) UPC 841548000028 packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Procaps S.A. de C.V.
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.