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 Nov 11, 2015
Robotic Arm Interactive Orthopedic (RIO) system component PN#205143 (locking pin) and PN# 112220 (connector). Indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Nov 4, 2015
Signature Patient-Specific Surgical Guides; patient specific instruments used as a guide during surgical procedure for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Materialise N.V.
FDA (openFDA device enforcement)
Reported Oct 28, 2015
AltiVate Humeral Socket Shell Trial, Part Number 804-06-052 The glenoid baseplate is intended for cementless…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Oct 21, 2015
Monode, Shortwave Accessory Model #: 02200002 Used in conjunction with the Intelect Shortwave Diathermy 100 and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
FDA (openFDA device enforcement)
Reported Oct 14, 2015
Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Oct 7, 2015
Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lifeline Systems, Incorporated
FDA (openFDA device enforcement)
Reported Sep 30, 2015
Disposable Reflective Marker Spheres The Disposable Reflective Marker Spheres used in conjunction with a stereotaxic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Sep 30, 2015
The Leica ASP6025 Tissue Processor. Pathology and Hematology Departments. The Leica ASP6025 Tissue Processor is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Sep 23, 2015
The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology Departments. The Leica ASP200S/ASP300S Tissue…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Sep 23, 2015
XGAUZE Trauma Dressing, catalog number FIN-0002-01. XGAUZE is a 3" x 36" z-folded rayon/polyester dressing embedded…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Revmedx Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2015
MEDIVATORS HEMOCOR HPH700, HPH-1400TS, HPH-1000TS. Enables the perfusionist to manage the patient's hematocrit and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2015
Ropivacaine HCl 0.2% in 100 mL total volume in a 100 mL Yellow Cassette Res. Flowstop in Sodium Chloride 0.9%, Rx Only,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pharmedium Services, LLC
FDA (openFDA drug enforcement)
Reported Sep 16, 2015
CDI 500 Blood Parameter Monitoring System. Provides continuous, on-line monitoring of the extracorporeal partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Sep 9, 2015
A&W Cream Soda 12 FL OZ (355 mL)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dr. Pepper Snapple Group Inc.
FDA (openFDA food enforcement)
Reported Sep 9, 2015
think Thin Protein & Fiber Oatmeal, Madagascar Vanilla, Almonds, Pecans; 10 g Protein, 5 g Fiber, 190 calories; Net wt…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Interpac Technologies
FDA (openFDA food enforcement)
Reported Sep 9, 2015
Big Train Chai Tea Vanilla Chai, Naturally and Artificially Flavored Drink Mix, No Sugar Added, NET WT 56 oz (3 LB 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerry Foods
FDA (openFDA food enforcement)
Reported Sep 9, 2015
Neptune 2 Waste Management System Docking Station (120V and 230V), New and Refurbished Product Usage: The Stryker…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Sep 2, 2015
ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be used to place patients at an accurately…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Centricity PACS-IW with Universal Viewer Product Usage: The Centricity PACS-IW with Universal Viewer is a picture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Kale Crisps Zen Nori product is seaweed flavored dehydrated kale chip, sold under brand Veggie Evolution, each poly…
High riskUsing this product could cause serious injury, illness or death — stop using it now.It Takes A Village Foods, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2015
Kroger Ground Cinnamon UPC 11110 70034 NEW WT. 18.3 oz Plastic container
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Getinge 86 Series Washer/Disinfector with G1 control system software, Model 8666 and Model 8668. For use in healthcare…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Getinge Disinfection Ab
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 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.