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 May 16, 2018
Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported May 16, 2018
Dragon Ultra Ehanced Indo Extract 4-ct x 500 mg capsules in pouches.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maya Distribution, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported May 16, 2018
Jasper Vektor, Class II Correction Appliance, Part No. 610-500 used for correcting class 2 malocclusions by applying…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TP Orthodontics, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported May 9, 2018
StoneBreaker Pneumatic Lithotripter, Catalog number: SBL-KIT1; GPN: G52604 UDI:(01)00827002526044
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported May 9, 2018
Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported May 2, 2018
Advance¿ 35LP Low-Profile PTA Balloon Dilatation Catheter; Catalog numbers: PTA5-35-135-6-2 .0 and PTA5-35-135-4-4 .0;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Divinity Product Distribution LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 18, 2018
VOLISTA StandOP Surgical Light; Model numbers VLT600 SF AIM STP, VLT600 DF AIM STP, Ref. codes ARD568811901,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge US Sales LLC
FDA (openFDA device enforcement)
Reported Apr 18, 2018
AUTO REF/KERATOMETER ARK-1s
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nidek Inc.
FDA (openFDA device enforcement)
Reported Apr 11, 2018
HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box, each catheter is packaged in an individual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Ventilator System including Pediatric-Adult…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 4, 2018
(1) Sigma HP Cemented Trochlea Size 1 Narrow Left, Catalog Number: 102403100, GTIN: 10603295001614; (2) Sigma HP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Apr 4, 2018
Gas Module 3 monitoring spirometer, Part Number: 115-030108-00 Product Usage: The Gas Module 3 is an accessory device…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Mar 28, 2018
BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 (UDI: 50382903664011); 2. 366450 (UDI:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 21, 2018
NovaKone Daily Wear Soft contact; Catalog Number: AONKS54 Product Usage: The NOVAKONE SPHERICAL lens is indicated for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alden Optical
10 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 21, 2018
Kodiak Cakes, Energy Waffles, Blueberry Chia, Net Wt 10.72 Oz (304 g), Kodiak Cakes, Park City, UT. Packaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kodiak Cakes, LLC
FDA (openFDA food enforcement)
Reported Mar 21, 2018
OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Medical Corporation
FDA (openFDA device enforcement)
Reported Mar 14, 2018
i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Point Of Care Inc.
FDA (openFDA device enforcement)
Reported Mar 14, 2018
O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog Number: B1-700-02000 The O-arm O2 Imaging System is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Mar 14, 2018
cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 +…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
2.5 mm Reaming Rod, Ball tip, 950 mm, sterile, Part Number: 351.706S Reaming Rods are intended for guiding of reamers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Flexible Shaft hip and anatomical shoulder instrument used for preparation of bone in Trauma, Hip and Shoulder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, 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.