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.

1,581 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 Nov 29, 2023

BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…

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

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 29, 2023

EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

Novum IQ Syringe infusion system, Product Code 40800BAXUS

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

BD Alaris PCU REF 8015

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 15, 2023

StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The StealthStation System, with StealthStation…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 8, 2023

Smiths Medical Portex Bivona Pediatric Tracheostomy Tube, Cuffless, Model 60P045, Sterile.

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

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005

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

Acclarent, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 1, 2023

Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

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

Cardinal Health 200, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 1, 2023

Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate flavor

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

Orgain

FDA (openFDA food enforcement)

Medical devices

Reported Oct 25, 2023

Monoject(TM) 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack, Model Number/Product Code: 1180100777

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

Cardinal Health 200, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 18, 2023

Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced Surgery Center SAR, Sterile. (2) Presource Block…

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

Cardinal Health 200, LLC

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 18, 2023

Evivo with MCT Oil Infant Probiotic Activated B. infantis EVC001 (ActiBif) For Enteral or Oral Administration…

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

Infinant Health, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 18, 2023

CellQuicken Analyzer (Smart-Watch and Software), RoyalVibe Ultrasound Generator, Brainvibe, Envirovibe Water…

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

RoyalVibe Health Ltd.

FDA (openFDA device enforcement)

Food

Reported Oct 18, 2023

LittleOak Natural Goat Milk Infant Formula (Stage 1); packaged in 800g (1.8lbs) tin cans - six cans per case.

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

The Little Oak Company Ltd.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 27, 2023

Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…

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

Abbott Medical

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 13, 2023

ISee Ortho-K Lens

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

PARAGON VISION SCIENCES, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 5, 2023

AJC International, Inc. Recalls Frozen, Raw Pork Products Imported Without Benefit of Import Reinspection

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

AJC International, Inc.

USDA FSIS

Food

Reported Aug 23, 2023

Tim Heung Yuen Black Melon Seed 6 oz., 12 oz. Ingredients: Melon Seeds, Salt, Sugar & Anise Seed Distributed By Richin…

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

Richin Trading Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 16, 2023

HoverMatt, 39" W x 78" L, REF: HM39SPU-B

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2023

OEC Flexiview 8800 Systems with 9-inch Image Intensifier

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

GE OEC Medical Systems, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 9, 2023

VERITAS Advanced Infusion Packs (VRT-AI) and VERITAS Advanced Fluidics Packs (VRT-AF)

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

Johnson & Johnson Surgical Vision, 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.