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.

2,136 stored notices name Idaho, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Idaho too — those are in the archive.

Medical devices

Reported Mar 26, 2025

Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLine H Set & VitaLine H…

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

Oridion Medical 1987 Ltd.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 26, 2025

Chocolate Peanut Butter Protein Balls. Product has expected life of 2 weeks and does not require refrigeration. Product…

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

Prep'd CDA LLC

FDA (openFDA food enforcement)

Medical devices

Reported Mar 19, 2025

Brand Name: Da Vinci 5 Product Name: ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals Model/Catalog Number: 380730 Software…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 19, 2025

Stryker CinchLock Flex Knotless Anchor with Inserter and Suture, REF CAT02643, Sterile EO, Rx Only MR Safe CE 0197

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

Stryker Corporation

FDA (openFDA device enforcement)

Food

Reported Mar 19, 2025

Black Beans, Dried, net wt. 16 OZ (1 LB) 454g, packaged in plastic bag. Packaged in the U.S. UPC 0 70552 70412 1.…

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

Trinidad Benham Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 19, 2025

Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-00A, (2) G5A-01A, (3) G5A-02A, (4)…

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

ZOLL Medical Corporation

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Access Erythropoietin (EPO), Catalog Number - A16364 a glycoprotein (~30,400 Daltons) produced primarily by the kidney,…

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Paradigm REF: MMT-712 and MMT-715

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

Medtronic MiniMed, Inc.

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 12, 2025

Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3-027-350-14,…

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

Micro Therapeutics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 12, 2025

Item #96507 and item# 32901, King Harvest Balsamic Hummus, net wt. 10oz., UPC 025726 310097, perishable and…

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

Pacific Coast Fresh Co.

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 5, 2025

DxC 500 AU Clinical Chemistry Analyzer, REF: C63519, and C63520 with affected software.

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

Beckman Coulter Laboratory Systems (suzhou) Co., Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 5, 2025

BD Pyxis: MedFlex, REF: 1119-00; MedBank Tower REF: 1145-00; MedBank MedPass, REF: 139088-01 and associated BD Pyxis…

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

CareFusion 303, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 5, 2025

5912MOD-CAU 11" Gluten Free Friendly Cauliflower Shell; Bulk packaged in a blue poly bag, within a corrugated box. 20…

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

Deiorio Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 5, 2025

Brand Name: Leica Biosystems Cryostats Product Name: CM1950 Model/Catalog Number: 1491950C4US Software Version:…

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

Leica Biosystems Nussloch GmbH

FDA (openFDA device enforcement)

Food

Reported Mar 5, 2025

Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER…

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

Nestle-USA, Inc. (Corporate Office)

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 26, 2025

3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 20cm System Kit, US…

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

Kci USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2025

LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo¿ RD rainbow Adt 8¿ SpCO, SpO2, and SpMet, Adult Adhesive Sensors REF…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2025

Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In…

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

HF Acquisition Co. LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2025

Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Dressing Gel Model/Catalog Number: 31815 Software…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2025

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+…

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

Max Mobility LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2025

Nestle Toll House Valentine's Chocolate Chip cookie dough, Makes 20 cookies. Net wt 14 oz. UPC 0 28000-34408 5.…

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

Target Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2025

Temporary Titanium Abutments

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

DDS Lab

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general…

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

Ethicon, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Indicated for use in a hospital and in outpatient care…

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

Fresenius Kabi USA, LLC

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.