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.
1,689 stored notices name Montana, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach Montana too — those are in the archive.
Reported Apr 17, 2019
Impossible Foods Bulk, 5 lb. vacuum sealed plastic-pack. Keep Frozen; This is a plant product that is looks like and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Impossible Foods
FDA (openFDA food enforcement)
Reported Apr 17, 2019
syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Planning and syngo CT.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2019
Laparotomy Sponge with the following product description and model numbers: 1. Lap 18X18 XR (5 each/pack, 20 pack/case)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2019
BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 13, 2019
Big Daddy s Bold Cheese Pizza, item No. 78985. 3-Pack. Contains 9-44.53 oz. Pizzas. Net Wt. 25.04 Lbs. (11.36 kg) For…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schwan's Global Supply Chain, Inc., Specialy Foods Plant
FDA (openFDA food enforcement)
Reported Mar 13, 2019
Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Phoenix AST-s Indicator, Catalog Number 246009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Feb 27, 2019
AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
TRINIAS for diagnostic imaging and interventional procedures in cardiac angiography, neurovascular angiography,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems USA Com
FDA (openFDA device enforcement)
Reported Feb 20, 2019
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Culinary Secrets, Butterscotch Instant Pudding Mix, Net Wt. 28 OZ, Marketed by Independent Marketing Alliance, Houston,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Diamond Crystal Brands, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
FDA (openFDA device enforcement)
Reported Feb 13, 2019
ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Italian Tapenade sandwich is Hoagie sandwich made with pepperoni, salami, capicola, cheese, Tapenade spread and green…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Spokane Produce Inc.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 16, 2019
Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
2 more products in this recall
FDA (openFDA device enforcement)
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)
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)
Reported Jan 2, 2019
Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit per Cavity #3 Cavity Deep/20 pieces per case…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
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)
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)
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)
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)
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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.