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 22, 2023

Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM, REF: 1610MSK; 18G x 16CM, REF: 1816MSK

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 22, 2023

Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box

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

Keurig Dr Pepper

FDA (openFDA food enforcement)

Medical devices

Reported Mar 15, 2023

LATITUDE NXT Remote Patient Management System, LATITUDE NXT System Server Software Model 6460.

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2023

PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic…

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

Preat Corp.

FDA (openFDA device enforcement)

Meat & poultry

Reported Mar 10, 2023

FSIS Issues Public Health Alert for Trader Joe’s Chicken Salad Due to Misbranding and an Undeclared Allergen

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Taylor Farms Northwest LLC

USDA FSIS

Food

Reported Mar 8, 2023

HEILEMANN CONFISERIE WEHNACHTSFIGUREN AUS EDELVOLLMILCH-SCHOKOLADE Solid Chocolate Holiday Treats 3.5 oz box UPC…

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

Alpenland International, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 8, 2023

Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2023

DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagnostic quality…

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

Carestream Health, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2023

The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 8, 2023

Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 8, 2023

AxiEM" Non-Invasive Patient Tracker

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 18, 2023

Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400, Female Lock - Female Lock Guarded Luer Connector,…

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

International Medical Industries, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 4, 2023

Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…

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

Acumed LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2022

The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set…

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

Natus Medical Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Dec 28, 2022

X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.

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

NuVasive Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 28, 2022

Red Button Vintage Creamery French Silk Pie, Net Wt. 31.88 oz. (904g), in a clear plastic dome and black plastic base,…

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

Rocky Mountain Pies, LLC

FDA (openFDA food enforcement)

Food

Reported Dec 21, 2022

Sardines in tomato sauce packed in cans labeled in part, "WILD PACIFIC SARDINES RAINCOAST TRADING TM***IN TOMATO…

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

St. Jean's Coast Mountain Resources Ltd. (dba) St. Jean's Ca

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2022

Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044

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

Intersect ENT, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2022

Alcon Custom Pak Surgical Procedure Pack

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

Alcon Research, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

MicroScan autoSCAN-4 Instrument, Catalog Number B1018-280

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

Beckman Coulter, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2022

Hamilton-C6

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

Hamilton Medical AG

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2022

Pedialyte Unflavored Electrolyte Solution 2 fl oz plastic reclosable bottle 12-4 packs in a case

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

Abbott Laboratories

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2022

Extension Tabletop for Operating Table System 1140, Model Nos. 1140.20F0 and 1140.20AN

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

Getinge USA Sales Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2022

Philips Laser System, REF: LAS-100. Used in minimally invasive interventional procedures within the cardiovascular…

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

Spectranetics Corporation

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.