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 Feb 11, 2026
JUICE from the Raw, DETOX GREENS
High riskUsing this product could cause serious injury, illness or death — stop using it now.Everpress Juice
6 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 11, 2026
Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2026
Product is Frozen Half Shell Oysters in 15-16 pound blocks. Packaged in generic brown cardboard boxes. Side panel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Khee Trading, Inc.
FDA (openFDA food enforcement)
Reported Feb 11, 2026
MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Feb 11, 2026
WinCo Foods Deli Margherita Pizza Thin Crust, Item #67279. Net wt. 17oz. UPC 0267279 807987. Product is Take & Bake and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WinCo Foods LLC
FDA (openFDA food enforcement)
Reported Feb 4, 2026
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cerapedics, Inc.
FDA (openFDA device enforcement)
Reported Feb 4, 2026
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LSL Healthcare Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Ireland, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
SQ40S Blood Transfusion Filter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GVS TM, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 28, 2026
Philips Azurion system; Software Version Number: R3.1;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
FDA (openFDA device enforcement)
Reported Jan 21, 2026
FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott Diabetes Care, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2026
Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Kabi USA, LLC
FDA (openFDA device enforcement)
Reported Jan 21, 2026
CentriMag Blood Pump, REF: 102953, 201-20003, 201-90010, 201-90016; CentriMag RVAD HDE KIT, REF: 104318; CentriMag…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
FDA (openFDA device enforcement)
Reported Jan 14, 2026
BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 Count per Lb. Net wt. 32oz (2LB).…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Direct Source Seafood LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 14, 2026
Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2026
Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McCain Foods USA Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 14, 2026
Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remote Diagnostic Technologies Ltd.
FDA (openFDA device enforcement)
Reported Jan 14, 2026
The Pressio 2 ICP Monitoring System, Model Number PSO-4000; Intracranial Pressure Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sophysa
FDA (openFDA device enforcement)
Reported Jan 7, 2026
Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, LLC
FDA (openFDA device enforcement)
Reported Dec 31, 2025
BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system reagent for the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Ireland, Inc.
FDA (openFDA device enforcement)
Reported Dec 31, 2025
BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Idaho recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.