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Recalls distributed in Idaho

These notices name Idaho 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.

2,107 stored notices name Idaho, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Idaho too — those are in the archive.

Medical devices

Reported Mar 2, 2022

NobelReplace Conical Connection RP 4.3x11.5 mm REF 36707 STERILE R

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

Nobel Biocare USA LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 23, 2022

RNAstill Molecular Transport Medium Vial, Catalog number MTM-001, a component of the following catalog numbers of…

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

Base 10 Genetics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 23, 2022

bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. The bellavista…

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

Vyaire Medical

FDA (openFDA device enforcement)

Food

Reported Feb 16, 2022

Ahold 10oz Chopped Romaine Product UPC 688267011085

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

Dole Fresh Vegetables Inc.

75 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 2, 2022

Bake Crafters - Maple Waffle WG Chicken Sausage Packaged into cardboard containers 126 units per case

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

Bake Crafters

FDA (openFDA food enforcement)

Food

Reported Feb 2, 2022

Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually

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

Brownie Points LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 2, 2022

GE Vscan Extend, being sold as "Vscan Extend Console"

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

GE Healthcare, LLC

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 2, 2022

GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal…

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

World Health Products LLC

FDA (openFDA food enforcement)

Food

Reported Jan 19, 2022

Boba Origin Brown-Sugar Milk Tea 100% WHEY PROTEIN ISOLATE 5.5g BCAA INGREDIENTS: Whey Protein Isolate, Black Tea,…

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

NutraCap Labs LLC

105 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 5, 2022

iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States);…

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

AMO Manufacturing USA, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

RAPID 20 E, REF 20701, System for the identification of Enterobacteriaceae in 4 hours, 25 strips/package, IVD.

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

Biomerieux Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z

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

Acclarent, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial,…

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

Medtronic Navigation, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.

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

Wright Medical Technology Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

MENTOR Saline-Filled Breast Implants are constructed from room temperature vulcanized silicone elastomer, made of…

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

Mentor Texas, LP.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use

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

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 15, 2021

O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model preparation for tooth…

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

Orchestrate Orthodontic Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 15, 2021

OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control…

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

Osteomed, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog…

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

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 8, 2021

NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product…

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

NuVasive Specialized Orthopedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 1, 2021

ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17…

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

Abbott Laboratories

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 24, 2021

Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes…

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

Fujifilm Irvine Scientific, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

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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.