All recall categories

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.

Medical devices

Reported Apr 19, 2017

Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 12, 2017

DX-D600 - DXD Imaging Package

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

AGFA Healthcare Corp.

FDA (openFDA device enforcement)

Food

Reported Apr 5, 2017

Baidyanath brand Sarivadi Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Butala Emporium, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 29, 2017

Raindrop Near Vision Inlay, Model# RD1-1

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Revision Optics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 22, 2017

BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 22, 2017

Frozen Raw Bay Scallops, packaged in a clear 5 lbs. bag, (six bags per case or total 30 lbs. case), food service…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sea Port Products Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 22, 2017

Terumo Advanced Perfusion System 1-Level Sensor II Pads, Product Usage: Ultrasonic couplant used to facilitate the…

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)

Medical devices

Reported Mar 22, 2017

Toshiba Kalare DREX-KL80 X-ray generator

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Toshiba American Medical Systems Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2017

Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2017

Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition, Circle Collection, Lunatic, Fright,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The See Clear Company

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

BD AffirM VPIII Microbial Identification Test

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cook Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

McKesson Radiology 12.2 - Picture Archive Communication System (PACS)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mckesson Medical Imaging

FDA (openFDA device enforcement)

Food

Reported Feb 22, 2017

Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bwi Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 22, 2017

LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The Modular Revision Femoral hip stem is made up of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Encore Medical, LP

FDA (openFDA device enforcement)

Food

Reported Feb 22, 2017

Pizza Hut Creamy Alfredo sauce, case size 40 lbs. 8 bags per case. Bags are each 80 oz (5 lbs) of sauce

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Yum Retaurants International

FDA (openFDA food enforcement)

Medical devices

Reported Feb 15, 2017

Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Bariatric Bed - BAR600IVC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Invacare Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merge Healthcare, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Teleflex Medical

FDA (openFDA device enforcement)

Drugs

Reported Feb 15, 2017

Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

VistaPharm, Inc.

FDA (openFDA drug enforcement)

Food

Reported Feb 8, 2017

Kings Pastry Tuxedo Bar Cake (12" x 4"), 1050 g Product Code: 10038 UPC: 685961100381

High riskUsing this product could cause serious injury, illness or death — stop using it now.

King's Pastry

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 1, 2017

FRONT: Stauffer's Animal Crackers Original; Net Wt. 32 OZ.; BACK: (best by date): 07SEP17; (bag lot numbers) LC120716…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

D. F. Stauffer Biscuit Co., Inc.

FDA (openFDA food 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.