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.
1,582 stored notices name Hawaii, reported between Jun 27, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.
Reported Aug 2, 2017
STOCKERT Heater-Cooler System 3T, 230 V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Pacific Wave Frozen Tuna Loins; 30# case. Imported by Unified Seafood Co., Inc. www.unifiedseafood.com
High riskUsing this product could cause serious injury, illness or death — stop using it now.Unified Seafood Company., Inc.
FDA (openFDA food enforcement)
Reported Jul 19, 2017
Ultrasonic Endoscope Model Number EG-530UT A flexible ultrasonic endoscope intended to provide ultrasonic images of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujifilm Medical Systems U.S.A., Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Pacific Wave Yellow Fin Tuna loins; 30 lb. cases. Product of Indonesia; Imported by Unified Seafood Co., Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.P & E Foods Inc.
FDA (openFDA food enforcement)
Reported Jul 12, 2017
Logic Fit Tibial Tamp Head
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Nussloch GmbH ASP6025 Tissue Processor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Exactech 1.5" Novation Calcar Planer Guide Tip To assist the surgeon in the implantation of Novation hip system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Jul 5, 2017
Pointe Scientific CRP(HS) Wide Range Control Set and Pointe Scientific CRP(HS) Wide Range Standard Set 5 Levels of 1 x…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medtest Holdings, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 5, 2017
SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number: CH-200/CH-200M Holds an x-ray tube unit and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems USA Com
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 28, 2017
Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 21, 2017
Philips DigitalDiagnost 3.1.x X-Ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 7, 2017
The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jun 7, 2017
NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Dolphin Inflation Device, REF 0185NA. Rx only, Sterilized using Ethylene Oxide. DOLPHIN is a single-use, sterile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Ceftriaxone TX 32 US S30, Ref 412302 and Ceftriaxone TX 32 US F100, Ref 507058 ETEST is a quantitative technique for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 31, 2017
CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.RB Manufacturing LLC
FDA (openFDA food enforcement)
Reported May 31, 2017
Optic Splash (naphazoline hydrochloride) Eye Drops, packaged in 0.5 FL OZ (15mL) bottles, Manufactured by SATO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sato Pharmaceutical Inc.
2 more products in this recall
FDA (openFDA drug enforcement)
Reported May 31, 2017
Herbal Tea Variety 120 ml/pouch, 40 pouches/case
High riskUsing this product could cause serious injury, illness or death — stop using it now.U S Deer Antlers Export & Import
FDA (openFDA food enforcement)
Reported May 24, 2017
SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 24, 2017
ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 24, 2017
Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported May 24, 2017
NexGen Offset Stem Extension, sizes 14mm and 17mm For use in total arthroplasty.
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.