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 Sep 27, 2017
Dark Chocolate Jete Nutritional Energy Bar, One Mother of a Bar, Net wt. 61 gram. Product is package in a cellophane…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kelejete LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 20, 2017
Spectra-System/Legacy Guided Surgery Handle Kit, Device Listing Number D245883. The Guided Handle Kit (G-HK) allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 13, 2017
MOSAIQ Medical Charged-Particle Radiation Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
mcompass 2-channel Balloon Catheters The mcompass Biofeedback Anorectal Manometry System is for use on patients…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medspira, LLC
FDA (openFDA device enforcement)
Reported Sep 6, 2017
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Optovue, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 30, 2017
DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,
High riskUsing this product could cause serious injury, illness or death — stop using it now.NatureAll-STF Holding, LLC
7 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 23, 2017
Coconut Beverage, So Delicious brand, 1.89 liter carton.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Idaho Foodbank
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 9, 2017
Steamers in 5 Clams in Butter & Garlic Sauce, Goose Point brand. Product is packaged in a plastic tray with heat sealed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nisbet Oyster Co. Inc.
FDA (openFDA food enforcement)
Reported Aug 9, 2017
Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Professional Complementary Health Formulas, LLC
FDA (openFDA food enforcement)
Reported Aug 2, 2017
BioHealth Pasture Fed Precision Blend Time Release Protein: Cookies and Cream Flavor; Sold in 2 lb.(960G) UPC 6 42014…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innovative Nutrition Technologies
FDA (openFDA food enforcement)
Reported Aug 2, 2017
STOCKERT Heater-Cooler System 3T, 230 V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2017
MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Sooji Coarse, Siva's brand, packaged in 2 lbs. and 4 lbs poly bags. UPC for 2 lbs. package is 8 46499 00316 1 UPC for 4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Reshmi's Group Inc.
FDA (openFDA food enforcement)
Reported Jul 19, 2017
Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Simple truth Dry Roasted Macadamia Nuts 12 oz bags UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Corporate Food Technology Laboratory
FDA (openFDA food enforcement)
Reported Jul 19, 2017
Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oscor, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
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.