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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.

1,581 stored notices name Hawaii, reported between Jun 27, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Hawaii too — those are in the archive.

Medical devices

Reported Aug 4, 2021

ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom

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

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 4, 2021

Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of…

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

Sunrise Medical (US) LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, Closed Eyelet, REF AR-2323BCC

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at…

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

Cardinal Health 200, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

Cell Marque, RabMAb,CD17, c-kit (YR145) Rabbit Monoclonal Primary Antibody, REF: 117R-18, IVD, CE, GTIN: 00841683123798

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

Cell Marque Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an…

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

Respironics California, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as…

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

Canon Medical System, USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.

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

Owen Mumford USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…

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

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;

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

Medtronic Heart Valves Division

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems, Kappa Freie Leichtkette (Human) kit for Roche cobas…

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Food

Reported Jul 7, 2021

Guan's Seafood Mushroom - hetre blanc UPC 8 5926700750 1 150 g clear plastic package with green bottom; Product code…

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

California Terra Garden, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 23, 2021

Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 CPU is also used as spare part.

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

Radiometer Medical ApS

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 16, 2021

Atec Insignia Anterior Cervical Plate System, REF 136-0116, Insignia, ACP, 1-Level, 16 mm, Rx Only, Non-Sterile, UDI:…

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

Alphatec Spine, Inc.

28 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 16, 2021

Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS)…

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

Normand-Info S.A.S.U.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 16, 2021

RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 ,…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Jun 9, 2021

Change Healthcare Enterprise Viewer - Product Usage: intended to be used with off-the-shelf hardware for the 2D and 3D…

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

Change Healthcare Canada Company

FDA (openFDA device enforcement)

Food

Reported Jun 9, 2021

Mahayograj Guggulu; 120 Vegetarian Capsules, 1/2 lb. bags of powder Dietary Supplement, 1030 Matley Lane, Unit A Reno,…

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

Garry N Sun USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 2, 2021

IRON GEN 2: ROCHE COBAS INTEGRA ANALYZER, REAGENT CASSETTES, Catalog#: 03183696122 - Product Usage: In vitro test for…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported May 26, 2021

S&W Organic Black Beans, 15 oz. can, Distributed by: Faribault Foods, 3401 Park Ave NW, Faribault, MN 55021.

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

Faribault Foods

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 26, 2021

ISOMORPH 28 PURE WHEY iSOLATE BANANA CREAM PIE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89846 7 & 5LB, UPC 6 49241…

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

Hi Tech Pharmaceuticals

13 more products in this recall

FDA (openFDA food enforcement)

Food

Reported May 26, 2021

PUBLIC GOODS brand HAIR, SKIN, & NAILS Dietary Supplement; 60 tablets per bottle; Other ingredients: Stearic acid;…

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

Public Goods

FDA (openFDA food enforcement)

Medical devices

Reported May 26, 2021

GORE VIBIL Biliary Endoprosthesis: stents, drains and dilators for the biliary ducts. Catalogue numbers: VH1008040,…

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

W.L. Gore & Associates, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 19, 2021

PowerPort duo M.R.I. Implantable Port, with attachable 9.5F Polurethane Open-Ended Dual-Lumen Venous Catheter, REF…

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

Bard Peripheral Vascular Inc.

2 more products in this recall

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.