Recalls distributed in Hawaii
These notices name Hawaii 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.
1,581 stored notices name Hawaii, reported between Jun 27, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.
Reported Mar 25, 2026
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2;…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Winder Laboratories, LLC
FDA (openFDA food enforcement)
Reported Mar 18, 2026
DxC 700 AU, REF: B86444, B86446
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Mishima K.K.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057
Moderate riskThis product could cause temporary or reversible health problems — stop using it.International Life Sciences
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 18, 2026
PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2026
Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2026
Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2026
Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascutek, Ltd.
FDA (openFDA device enforcement)
Reported Mar 4, 2026
Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J2C Hawaii LLC
FDA (openFDA food enforcement)
Reported Mar 4, 2026
Fish Ball, Frozen, 40 pieces per pack, 200g Wt. UPC# 810093891338
High riskUsing this product could cause serious injury, illness or death — stop using it now.Min Jiang Food Store Inc. dba Koi Koi Trading
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 4, 2026
Prime Food Processing Dried Croaker Fish; NET WT: 8oz (227g); Ingredients: Croaker Fish, Salt; CONTAINS: FISH (CROAKER…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Prime Food Processing LLC.
FDA (openFDA food enforcement)
Reported Feb 25, 2026
Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 25, 2026
Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pure Solutions, Inc.
FDA (openFDA food enforcement)
Reported Feb 25, 2026
MOLLI 2 System System includes: MM1000 (Pack of 10) - MOLLI Introducer (8cm, 14G) and MOLLI Marker UDI (GTIN):…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
FDA (openFDA device enforcement)
Reported Feb 18, 2026
Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Costco Wholesale Corporation
FDA (openFDA food enforcement)
Reported Feb 18, 2026
Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 18, 2026
Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McCain Foods USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 18, 2026
Brilliance iCT; Product Code (REF): 728306;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 11, 2026
JUICE from the Raw, DETOX GREENS
High riskUsing this product could cause serious injury, illness or death — stop using it now.Everpress Juice
6 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 11, 2026
MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2026
Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk Magnifying Lens, Catalog VMD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vortex Surgical Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 4, 2026
INON ACE Antacid tablets (magnesium aluminosilicate, magnesium hydroxide and simethicone), 75-count bottle,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sato Pharmaceutical Co., Ltd.
FDA (openFDA drug enforcement)
Reported Jan 28, 2026
The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Ireland, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, 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.