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 Mar 14, 2018
O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog Number: B1-700-02000 The O-arm O2 Imaging System is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.-Littleton
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Mar 14, 2018
cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 +…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 14, 2018
2.5 mm Reaming Rod, Ball tip, 950 mm, sterile, Part Number: 351.706S Reaming Rods are intended for guiding of reamers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
6 more products in this recall
FDA (openFDA device enforcement)
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)
Reported Mar 7, 2018
Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant, Catalog Number D-TAP-MAX7-7 Dental implants are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 7, 2018
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO¿ is intended to be used for X-ray computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mobius Imaging, LLC
FDA (openFDA device enforcement)
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)
Reported Mar 7, 2018
ST AIA-PACK¿ PROG II, Progesterone II Assay, Part Number: 025239
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
1 more product in this recall
FDA (openFDA device enforcement)
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)
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)
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)
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)
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)
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)
Reported Feb 14, 2018
AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO is intended to be used for X-ray computed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Feb 14, 2018
ELWOOD FAT-FREE LOW SODIUM RANCH DRESSING ARTIFICIAL FLAVOR. Single serve.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elwood International, Inc.
FDA (openFDA food enforcement)
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)
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)
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)
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)
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)
Reported Jan 17, 2018
SHS Wel-Plan Wheat and Corn Strach Baking Mix , 400 g box,Cardboard carton, 18 cartons per case, but distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutricia North America
FDA (openFDA food enforcement)
Reported Jan 17, 2018
Sundream 12 V tanning bed
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ProSun International, LLC
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.