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 21, 2018
Chef Sensations Fire Roasted 1/2" diced onion/pepper blend Net Wt 20 lbs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Wornick Company
FDA (openFDA food enforcement)
Reported Nov 21, 2018
Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2018
VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Nov 14, 2018
EZ1 Advanced XL, Model Number: 9001492, GTIN: 04053228010760 Product Usage: The EZ1 Advanced XL is designed to perform…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Nov 7, 2018
EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 7, 2018
Zilver 518 Biliary Stent 4mm x 20mm, Catalog Number: ZIB5-125-4.0-20 Product Usage: The Zilver 518 and 635 Biliary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Medical Incorporated
38 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Boston Scientific Maestro 4000 Cardiac Ablation System, Firmware Version 5.14, Model Numbers: M00440000, M0044000D0,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Oct 31, 2018
J-Plasma Precise 360, single use, disposable. The Bovie J-Plasma Precise 360 Handpiece is used for the delivery of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bovie Medical Corporation
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET WT. 35 OZ (980 g) Callie's Charleston Biscuits; 1895 Avenue…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Callie's Charleston Biscuits
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 31, 2018
Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modality that produces…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Mitek Screw and Washer Depth Gauge, Product Code 219024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ecolab Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Medacta International MiniMAX CEMENTLESS ANATOMICAL STEM, 12/14: for cementless use in total or partial hip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medacta USA Inc.
FDA (openFDA device enforcement)
Reported Oct 31, 2018
O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number Bl70000027 Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
9 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2018
GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2018
La Mexicana Hot Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 128 oz. Gourmet Style Hot Salsa 16 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.La Mexicana LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 24, 2018
Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Switzerland GmbH
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Affixus Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180 Product Usage: Intended for the fixation of fractures
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
47 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2018
SK Food Group Recalls Chicken Products due to Possible Salmonella and Listeria monocytogenes Contamination in Vegetables
High riskUsing this product could cause serious injury, illness or death — stop using it now.SK Food Group
USDA FSIS
Reported Oct 17, 2018
Codan Filter (Codan catalog number BC 693) used with Medrad Patient Administration Sets (PAS) and Intego PET Infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Colpo-Pneumo Occluder, Part CPO-6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Mary's Harvest Fresh Foods, Inc. Recalls Wrap and Salad Meat Products due to Possible Salmonella and Listeria…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mary's Harvest Fresh Foods, Inc.
USDA FSIS
Reported Oct 17, 2018
NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neomed Inc.
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.