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 Dec 21, 2016
Performance-LOAD Ambulance Cot Fastener Stretcher, Wheeled
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Trader Joe's Mediterranean Hummus SKU #90642
High riskUsing this product could cause serious injury, illness or death — stop using it now.Two Chefs On A Roll, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 14, 2016
3M Universal Electrosurgical Pad, REF 9130 (100 pads / case) and 3M Universal Electrosurgical Pad with Cord, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Dec 14, 2016
MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a tool for tissue release of the transverse carpal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thayer Intellectual Property, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 18mm Item Code: 186850018 The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 30, 2016
LIAISON Estradiol II Gen, 310680, 310680-CN The DiaSorin LIAISON Estradiol II Gen assay is a chemiluminescent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diasorin Inc.
FDA (openFDA device enforcement)
Reported Nov 30, 2016
Pathfast D-Dimer, Reference number: PF1051-KUS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lsi Medience Corporation
FDA (openFDA device enforcement)
Reported Nov 23, 2016
Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCain Foods USA
FDA (openFDA food enforcement)
Reported Nov 23, 2016
Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported Nov 23, 2016
RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Nov 16, 2016
Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Surgical Inc.
FDA (openFDA device enforcement)
Reported Nov 9, 2016
Xhibit Central Station, Model 96102. Intended use is to provide clinicians with central monitoring of adult, pediatric…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
4205 Journey Rolling Walker Product Usage: used to assist people in walking
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US, ex-tem. Used to monitor the coagulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TEM Systems Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Awareness Corporation
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Product is refrigerated Boars Head To Go (BTG) Superfood Wrap, sold at deli department. The wraps are made in store…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fred Meyers Inc.
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Oct 26, 2016
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Oct 26, 2016
FI Dry Blueberry / Strawberry Blend, Product Code 21585. 40 lb corrugated case with polyliner. Manufactured by:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.QualiTech, Inc.
17 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Sagittal Blade 18.0X0.97X90MM, Model Number: 6118-097-090 Product Usage: Heavy duty Sagittal Blades are used to cut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFlow Thermal Pulsation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tearscience, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Calix P PEEK Lumbar System, PLIF Rasp
Moderate riskThis product could cause temporary or reversible health problems — stop using it.X Spine Systems Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2016
BioSentry Tract Sealant System, Product Code: 768022019S; Indicated to provide accuracy in marking a biopsy location…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Surgical Specialties Mexico S DE RL DE CV
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.