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.
Reported Aug 15, 2018
Grizzlies Brand and Grizzlies Granolas Oregon Trail Mix consisting of chocolate chips, fruit, seeds, and nuts. Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Green Valley Group, LLC
FDA (openFDA food enforcement)
Reported Aug 15, 2018
Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Aug 15, 2018
Seattle Sourdough Pub Buns 6 pack, net wt. 16 oz., UPC 0-72220-10164-5
High riskUsing this product could cause serious injury, illness or death — stop using it now.Portland French Bakery L T D
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 15, 2018
Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Water Pik, Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cayenne Medical Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 8, 2018
XLTEK EMU40EX EEG Headbox
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Nicolet¿ Ambulatory EEG
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
FDA (openFDA device enforcement)
Reported Aug 8, 2018
Diet Pepsi 7.5 oz cans, 6-pack. UPC on case label is 0 12000 16314 2. The product's case label is read in parts:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pepsico Inc.
FDA (openFDA food enforcement)
Reported Aug 1, 2018
Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Medical Division
FDA (openFDA device enforcement)
Reported Aug 1, 2018
ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Aug 1, 2018
Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Aug 1, 2018
BLAST Bandage, sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tactical Medical Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2018
T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems Ultrasound & Primary Care Diagnostics, LL
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intel-GE Care Innovations LLC
FDA (openFDA device enforcement)
Reported Jul 25, 2018
VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP; ARD568821961 VLT600DF AIM STP QL; ARD568811911 VLT600SF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet SAS
FDA (openFDA device enforcement)
Reported Jul 25, 2018
UNI-CP, Model Numbers: 330021S, 330023S, 330025S, 330030S, 330025S, 30030S, 330217S, 330220S, 330225S, 330230S,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NewDeal SA
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2018
RayStation stand-alone software treatment planning system, RayStation 4.5, RayStation 4.7, RayStation 4.9 (RayPlan 1),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Dimension Vista¿ CTNI Sample Diluent, KD692, SMN# 10445205
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 25, 2018
t:slim G4 Insulin Pump with Dexcom G4 Platinum CGM Software version: 4.3.4.3, Firmware version: 004722, Firmware, Fuel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tandem Diabetes Care Inc.
FDA (openFDA device enforcement)
Reported Jul 25, 2018
Naked Bread Hamburger Buns #NothingToHide, 8 pack. Product is packaged in low density polyethylene bag and identified…
High riskUsing this product could cause serious injury, illness or death — stop using it now.United States Bakery Corp.
FDA (openFDA food enforcement)
Reported Jul 18, 2018
BioMerieux mini VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 11, 2018
WATERMELON CHUNKS 6/9.5Z, 9.5 oz., UPC: 81851301386; WATERMELON SPEAR 6/16Z, 16 oz., UPC: 81851301591; WATERMELON SPEAR…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Caito Foods Service, Inc.
25 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 11, 2018
microTargeting" Drive System, Product Number MT-DS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FHC, Inc.
14 more products 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.