Recalls distributed in Montana
These notices name Montana 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.
1,662 stored notices name Montana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Montana too — those are in the archive.
Reported Feb 9, 2022
Wayfare Dairy Free Butter Salted & Whipped,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.WayFare Health Foods, LLC.
FDA (openFDA food enforcement)
Reported Feb 2, 2022
Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brownie Points LLC
FDA (openFDA food enforcement)
Reported Feb 2, 2022
GE Vscan Extend, being sold as "Vscan Extend Console"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 2, 2022
Trilogy Evo, Material Numbers DS2110X11B (USA) and KR2110X15B (Korea) The Trilogy Evo ventilator provides continuous or…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 26, 2022
VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jan 26, 2022
ZOCALO AJI LIMO DRIED CHILI PODS- ORGANIC, Dried Aji Peppers for consumer consumption. Product is vacuum sealed in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Power Selles Imports dba Culinary Collective
FDA (openFDA food enforcement)
Reported Jan 19, 2022
Flat Panel Detector, Model Number: TFP-800A, used with the Alphenix Systems, Item Numbers: INFX-8000V, INFX-8000C,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 5, 2022
iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States);…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AMO Manufacturing USA, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 5, 2022
Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Dec 29, 2021
Skinny Needle with Chiba Tip. RPN 090010, 090010-ET; GPN G14254, G15290. Rigid needle available with EchoTip to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Dec 29, 2021
Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Navigation, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 22, 2021
MENTOR Saline-Filled Breast Implants are constructed from room temperature vulcanized silicone elastomer, made of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas, LP.
FDA (openFDA device enforcement)
Reported Dec 22, 2021
Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Dec 15, 2021
SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Dec 15, 2021
Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mountain Meadow Herbs, Inc.
FDA (openFDA food enforcement)
Reported Dec 8, 2021
BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Dec 8, 2021
The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Magnolia Medical Technologies, Inc.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Specialized Orthopedics, Inc.
FDA (openFDA device enforcement)
Reported Dec 8, 2021
Classic Irish Coffee Hint of Cocoa, each packet weighs 1.09 oz (31g), 30 packets per case. UPC 8 60003 91545 5. This…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trail Toddy & Company LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 1, 2021
ARCHITECT i1000SR REF 01L86-01/1L86 and 1L87; ARCHITECT i2000SR REF 03M74-02/3M74; ARCHITECT i2000 REF 08C89-01/1G17…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 1, 2021
BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min (3660…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson Infusion Therapy Systems Inc.
FDA (openFDA device enforcement)
Reported Dec 1, 2021
Roberts Digital VIPR System (with E-size cylinder) Model: ROC-9840
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Western/Scott Fetzer Company
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 17, 2021
Hemodialysis Delivery System, Software Version 2.x.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Nov 17, 2021
NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal Jelly 1500mg 60 VCAPS (Distributed by Sofico) UPC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NOW Health Group Inc.
2 more products in this recall
FDA (openFDA food 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.