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.

2,107 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.

Medical devices

Reported Jan 16, 2019

Siemens Biograph Horizon PET/CT System, Product Usage: The Siemens Biograph systems are combined X-Ray Computed…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 2, 2019

Eat Smart Salad Shake Ups - Asian Sesame/Sesame Asiatique; 5.5 oz. (156 g); UPC 7 09351-30241 1, 7 09351 30244 2…

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

Apio, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 2, 2019

Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G…

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

Medtronic Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 2, 2019

Sea Salt Caramels Tumbled In Milk Chocolate, Moonstruck brand. The product sold in an individual resealable plastic…

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

Moonstruck Chocolate Company

FDA (openFDA food enforcement)

Medical devices

Reported Jan 2, 2019

RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6, RayStation 7 and RayStation…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Food

Reported Dec 26, 2018

Wegmans Roasted Corn and Bean Salad; 13 oz. Plastic Container, 40 oz. Plastic Container, 4.5 lb. Plastic Bulk Container

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

ASK Foods Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 26, 2018

enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual…

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

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2018

VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more of these susceptibility products: Catalog #…

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

bioMerieux, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons gloves are a…

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

Cardinal Health 200, LLC

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 26, 2018

Milk Chocolate Maltballs: NET Wt. 15 lbs. Item number 992 Case UPC 00797817-00992-9 Allergy Information: This product…

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

Marich Confectionery Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 19, 2018

UroLift System REF Catalog Number: UL400-4 Tray Contents: UroLift System with Handle Release Tool STERILE R CE 0050…

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

Neotract Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2018

Smartypants Kids Complete, Non GMO Multi and omega 3's vitamin D3 for bones, vitamin B12 for Energy: 90 gummies. UPC 8…

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

Smartypants Vitamins

FDA (openFDA food enforcement)

Food

Reported Dec 12, 2018

Tillamook Mudslide ice cream (item #63006), packaged in 3 gallon tub. UPC 0 72830 63006 1. The label is read in parts:…

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

Tillamook County Creamery Assoc

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 5, 2018

Ultra Dark Chocolate Amaretto Rainier Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261…

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

Chukar Cherry Company

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 28, 2018

The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Nov 28, 2018

Chocolate Cookies in plastic clamshell (12 count)

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

Cinnamon and Spice Bakery

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 28, 2018

Irrisept OR, Finished Bottle Assembly 450 ml STEP 1

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

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2018

Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon…

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

Merck Millipore Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code…

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

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System

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

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro…

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

Luminex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option

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

Stryker Medical Division

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.