All recall categories

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.

2,142 stored notices name Idaho, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Idaho too — those are in the archive.

Medical devices

Reported Aug 20, 2014

VIDAS D-Dimer Exclusion II, an automated quantitative test for use on instruments of the VIDAS family for the…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging

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

Biosound Esaote, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Codman Certas - In Line Valve Only; Product Code: 82-8800 The Codman Certas Programmable valve is an implantable device…

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

Codman & Shurtleff, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2014

Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2014

AdvanDx Quick FISH Fixation Kit for BC ( Blood Cultures), 50 tests. In vitro diagnostic. The QuickFISH Fixation Kits…

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

Advandx Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2014

Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…

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

Mckesson Medical Immaging

FDA (openFDA device enforcement)

Food

Reported Aug 6, 2014

Malt-O-Meal Frosted Flakes, item number 00955, UPC 42400-00955. Net Wt. 2.00oz (56g)

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

mom Brands

FDA (openFDA food enforcement)

Medical devices

Reported Aug 6, 2014

InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.

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

Stryker Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the…

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

DePuy Orthopaedics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

MK5 NX Controller--Wheelchair controller

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

Invacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

Sarns D4 Aortic Arch Cannulae 6.0mm, 7mm & 8mm angled and straight tip with or without side holes and/or luer Product…

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

Terumo Cardiovascular Systems Corporation

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2014

ACL TOP (Base), automated coagulation laboratory instrument.

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

Instrumentation Laboratory Co.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2014

There are 2 different labels for this same product with the same UPC. Label #1 Individual Bars: 100% natural Zing…

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

NW Nutritional Foods LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 23, 2014

e.cam camera system. Emission Computed Tomography System used to detect or image the distribution of radionuclides in…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2014

Certified Organic, Owl Canyon Whole Eggs, packed in one dozen and half-dozen cardstock packages, with a packing date of…

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

Six Dog, LLC

FDA (openFDA food enforcement)

Food

Reported Jul 16, 2014

Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red & Green Peppers, 19.4 oz 1 LB 3.4 oz), packed in…

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

Oregon Freeze Dry, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2014

The STERIS 4085 General Surgical Table Product Usage: is an electro-hydraulically operated surgical table designed to…

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2014

Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Jul 12, 2014

California Firm Recalls Chicken Products Due to Possible Salmonella Heidelberg Contamination

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

California Firm

USDA FSIS

Medical devices

Reported Jul 9, 2014

Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and…

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

Global Cooling Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2014

Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221

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

Microline Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2014

Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.

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

The Anspach Effort, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 2, 2014

Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System is intended to provide invasive or…

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

Nellcor Puritan Bennett Inc. (dba Covidien LP)

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.