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 Jul 27, 2016
Mountain Thins Trail Mix flavor, packaged in a stand-up film pouch (resealable), net wt. 5.3 oz. The UPC is 0 41770…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Brown & Haley Inc.
FDA (openFDA food enforcement)
Reported Jul 27, 2016
ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Kellogg's Special K Mini Brownies Blondie, 6 ct, 4.44 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg Company
24 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 27, 2016
RayStation 3.0, RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7 and RayStation 5 --- Radiation Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 27, 2016
Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Jul 27, 2016
HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
Duloxetine Delayed-Release Capsules, USP, 20 mg, 60-count bottles, Rx only, Manufactured by Apotex Inc, Toronto,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Apotex Scientific, Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 20, 2016
The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 20, 2016
cobas¿ Liat Influenza A/B Quality Control Kit; For use with cobas¿ Liat Influenza A/B Assay.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Molecular Systems, Inc.
FDA (openFDA device enforcement)
Reported Jul 20, 2016
6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 13, 2016
The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Ultrasonics, Inc.
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Novation Press-Fit Splined RDD, Extended Offset, HA Coated, 12/14 Taper Femoral Stems, Size 17. Product Usage Femoral…
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 Jul 13, 2016
GE Healthcare, Discovery MR750w
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jul 13, 2016
Natural Directions Organic Mixed Vegetables, frozen, net wt. 12 oz. UPC 0 15400 19672 7
High riskUsing this product could cause serious injury, illness or death — stop using it now.Norpac Foods, Inc. (Plant #8)
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 13, 2016
All 4-aminopyridine Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reliable Rexall-A Compounding Pharmacy
69 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 13, 2016
Synthes Ti Button Plate 7 Holes, Fastener, Fixation, nondegradable, Soft Tissue
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Jul 6, 2016
Reser's Deviled Egg Potato Salad, Refrigerated, Retail package, Net wt. 3 lbs. UPC 0 71117 00480 9; Reser's Deviled Egg…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc. - Century
7 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 29, 2016
Let's Talk Health Energizer Drink Mix Citrus 0.3oz UPC #91131180631
High riskUsing this product could cause serious injury, illness or death — stop using it now.Let's Talk Health, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 22, 2016
The XN-Series modules (XN-10, XN-20) are quantitative multi-parameter automated hematology analyzers intended for in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex Corporation
FDA (openFDA device enforcement)
Reported Jun 22, 2016
Universal Battery Charger II (UBC II)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
GE Revolution CT The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Philips Healthcare DigitalDiagnost stationary X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Healthcare
8 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Sedecal SA Mobile Diagnost w DR x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal USA, Inc.
FDA (openFDA device enforcement)
Reported Jun 15, 2016
Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
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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.