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.
1,551 stored notices name Hawaii, reported between Jun 27, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.
Reported Aug 19, 2015
Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mason Vitamins, Inc.
FDA (openFDA food enforcement)
Reported Aug 12, 2015
Merge Hemo, 9.10, 9.20.0, 9.20.1,9.20.2, 9.30, 9.40.0, 9.40.1, 9.40.2 with Massimo PHASEIN End Tidal CO2 (EtCO2)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2015
Raw Frozen Tuna Chunks Product of Indonesia. The bulk frozen tuna products can be identified from the Purchase Order…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Osamu Corporation
4 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 12, 2015
Whole Foods Market Raw Macadamia Nuts NET WT 11 oz (312g). UPC: 0-76958-62059-1, Distributed by Whole Foods Market…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
FDA (openFDA food enforcement)
Reported Aug 5, 2015
Invivo Expression MRI Patient Monitoring System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Jul 29, 2015
American Catheter / Cholangiogram Catheter 9100 Series.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Catheter Corp.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Bausch & Lomb SofPort Advanced Optics Aspheric Lens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Milex Vaginal-Hymenal Silicone Dilators Set of 4 P/N MX20 Product Usage: The CooperSurgical Milex Vaginal-Hymenal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
ADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests Product Usage: For in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (120V) 0702-001-000R, Repair Neptune 2 Rover…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Rifampin for Injection, USP 600mg/vial in a 20mL vial, Rx only, Manufactured for Fresenius Kabi LLC 3 Corporate Drive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Kabi USA, LLC
FDA (openFDA drug enforcement)
Reported Jul 15, 2015
Losartan potassium tablets USP, 25 mg, 90- count bottle, Rx only, Manufactured for Apotex Inc 150 Signet Drive, ON…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Apotex Inc.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 15, 2015
Breast Pack - contains Devon Light Glove Used during surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Healthcare, LLC.
50 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2015
LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Eating Right Black Bean Soup; 1.3 oz paper container. Dried soup to which consumer adds hot water. USPC: 79893-80026;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.San Francisco Spice Company, Inc.
FDA (openFDA food enforcement)
Reported Jul 1, 2015
Cambridge House Royal Smoked Salmon Sliced Side Products are packaged in Reduced Oxygen Package (ROP). Product is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Santa Barbara Smokehouse, Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 24, 2015
Amerigel Hydrogel Gauze Dressing 2 x 2, A5002. Wound Management.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
FDA (openFDA device enforcement)
Reported Jun 17, 2015
BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials…
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 Jun 17, 2015
Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Compass Health Brands
FDA (openFDA device enforcement)
Reported Jun 17, 2015
Rugby Poly Vitamin Liquid, 50ml
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmatech LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 10, 2015
Oncentra Brachy radiation therapy planning software designed to analyze and plan radiation treatments in three…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 3, 2015
100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2015
Elastic Ankle Support. A limb orthosis (brace) is a device intended for medical purposes that is worn on the upper or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.United Surgical Associates
2 more products in this recall
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Hawaii recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.