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 Mar 7, 2018

STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary, Secondary Administration Sets and Extension Sets (Catalog…

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

ConMed Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Agility with Integrity R3.2

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

Elekta Limited

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 7, 2018

Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System; Catalogue No: C7000 Product Usage: The…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 7, 2018

Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381

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

Seggiano USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 7, 2018

Zimmer Segmental System, ZSS Distal Femur. Sizes as follows: a. Size B-LT (Item No. 00585001201); b. Size B-RT (Item…

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

Zimmer Biomet, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2018

Innova Self-Expanding Stent System, 200 mm. Labeled with Material Number and description as follows: Product Usage: The…

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

Boston Scientific Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 28, 2018

IQF Green beans, sold as Not Ready To Eat (NRTE) product for use in foodservice or manufacturing applications. The…

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

National Frozen Foods Corporation--Seattle

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 28, 2018

Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled: 04961333232420) These instruments are…

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

Pentax

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter Chemistry Calibrators are intended for use when…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 21, 2018

WALNUT CREEK FOODS Caramel Popcorn NET WT 15 OZ (425g) Ingredients: Evaporated Can Juice, Popcorn, Butter (cream,…

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

Coblentz Distributing Inc. dba Walnut Creek Foods

FDA (openFDA food enforcement)

Medical devices

Reported Feb 21, 2018

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

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

GE Medical Systems China Co., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to…

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

Zimmer Biomet, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 21, 2018

A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily…

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

Zimmer Surgical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 14, 2018

Chobani Flip Key Lime Crumble - Key Lime Low-Fat Greek Yogurt with Graham Crackers & White Chocolate, 4-packs, 4/5.3 oz…

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

Chobani

FDA (openFDA food enforcement)

Medical devices

Reported Feb 14, 2018

Implant Direct, INTERACTIVE HEALING COLLAR, PART NUMBER 6530-15, 5.0mmL: 3.0mmD Platform

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

Implant Direct Sybron Manufacturing, LLC

FDA (openFDA device enforcement)

Food

Reported Feb 14, 2018

SunGlow, Unsalted European Style Butter Blend Margarine (16953 SNG), Net Wt 16 oz (1 lb) 454 g. Keep Refrigerated. UPC…

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

Ventura Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 14, 2018

DRILL BIT MINI QUICK CONNECT 1.0MM, REF 2312-20-200 & 2312-20-202, NON STERILE

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

Zimmer Biomet, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 7, 2018

IASA COLATURA DI ALICI DI CETARA ANCHOVY EXTRACT; 100 ml and 250 ml sizes; UPC 100 ml - 7 93232 54200 3; UPC 250 ml - 7…

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

Manicaretti Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 7, 2018

Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers Device is an endodontic root canal plugger.…

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

Ormco/Sybronendo

FDA (openFDA device enforcement)

Food

Reported Jan 31, 2018

Condies Foods Fresh Fruit, Item Number 40781, UPC 50777222655

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

Condies Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 24, 2018

ACCOLADE SR Pacemaker

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

Boston Scientific Corporation

23 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 24, 2018

Spice Supreme Beef Flavored Bouillon Cubes 1.7 oz (48 g) and NET WT. 3-1/2 OZ (98 g) 25 Count

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

Gel Spice Co., Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 24, 2018

Frozen Tuna Fillet Saku (Restaurant Supply Only); 22 lbs./2 x 5 kgs. Wild caught: Handline with Hook. Keep Frozen - 18…

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

H.I.G. Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Jan 24, 2018

Persona Partial Knee System, Size 8, Finishing Guide

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

Zimmer Biomet, Inc.

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.