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 Jan 1, 2014
Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm Imaging Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2013
Nature's Way, UPC 33674149263, Alive Whole Food Energizer with Iron, 60 Tabs 20009807; Nature's Way, UPC 33674149270,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schwabe North America, Inc.
12 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2013
17-P 1ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Main Street Family Pharmacy, LLC
298 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED SIZE 1-1.5 HP M.B.T. Keel Punch Knee Instrument is used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2013
Mozzarella String Cheese made with 2% milk for 1/4 less fat, sold under Kraft brand or Polly-O brand and packaged with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group
7 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 27, 2013
GE Healthcare Discovery NMCT 670, Discovery NM 630, Optima NMCT 640, & Brivo NM 615. The GE Discovery NMJCT 670 system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
CTF Brand Tapioca Pearl Pandan (Green Color), 14oz Plastic Bags, Packaged at 50 bags per case. Packaged in plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.N A Trading Inc.
FDA (openFDA food enforcement)
Reported Nov 27, 2013
VITROS Chemistry Products ACET Slides, 90 slides/pack; catalog number 1037274 VITROS Chemistry Products ACET Slides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
36 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
EPIQ 7 Ultrasound System, Model 795200, 795201, 795202. Intended for diagnostic ultrasound imaging and fluid flow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems North America Inc.
FDA (openFDA device enforcement)
Reported Nov 20, 2013
SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP LCD screen, 55074-2 revision B) Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 20, 2013
AW VolumeShare 4 (ADVANTAGE WORKSTATION 4.3.), AW VolumeShare 5 (AW VOLUMESHARE 5 WITH ANGIOVIZ OPTION), AW Server.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 13, 2013
Jim Dandy¿ Iron Fortified Quick Grits, 1lb paper box, Labeled in part "INGREDIENTS: IRON, WHITE CORN GRITS, NIACIN,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J M Smucker Co.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2013
Angel Food Cake; labeled for retail sale in the following stores: Safeway, Carrs, Dominicks, Genuardis, Pak N Save,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Safeway Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 13, 2013
Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre; 15248C-22/25 The Regional Anesthesia family of products is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
Baxter CLEARLINK System Non-DEHP Three Lead Extension Set. 6.0" (15 cm), 1.0 mL, Luer Activated Valve, male Luer Lock…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Nov 6, 2013
PIPELINE LS ACCESS SYSTEM, 15 Dilator, 5 mm, Insulated The PIPLINE LS Dilators and Holding Clip are intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare It
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2013
MAQUET Getinge Group CARDIOHELP Base Unit REF 70104.7999 REF 70104.8012 Manufactured for: MAQUET Cardiopulmonary AG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Medical Systems USA
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Disinfection
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Brilliance CT Big Bore Oncology, Brilliance CT Big Bore Radiology and Brilliance CT 16 (Air) Brilliance CT Big Bore…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 9, 2013
GE Healthcare, Discovery MR750 3.0T, Optima MR450w 1.5T, and Discovery MR450 1.5T . scanner designed to support high…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
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.