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.
Reported Mar 23, 2016
McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Sekure Chemistry Sekisui Diagnostics Acetaminophen L3K Assay, In-vitro Diagnostic Catalog Number: 506-10: R1: 1 x 10ml,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sekisui Diagnostics P.E.I. Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom) Powered stretcher
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Carys Dark Chocolate Almond Toffee with Hawaiian Salt. Product is packaged in printed cardboard packages in 1.3 oz , 4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cary's
FDA (openFDA food enforcement)
Reported Mar 16, 2016
Mobile wDR motorized portable diagnostic X-ray systems. Intended for use by a qualified/trained doctor or technologist…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sedecal S.A.
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Spacelabs Healthcare Xhibit Central Station, Model 96102 is used to provide clinicians with central monitoring of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2016
Braga Organic Farms Organic Pistachio Kernels, Raw; Certified Organic, USDA Organic. Packed in 8 oz. 1 lb. 2. lb and 5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Braga Organic Farms, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 9, 2016
Kopans Breast Lesion Localization Needle The Kopans Breast Lesion Localization Needle consists of a bevel-tip needle…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2016
BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 2, 2016
This reagent is for in vitro diagnostic use. Pax-5 (1EW) monoclonal antibody is intended to be used for the qualitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Feb 24, 2016
Dark Chocolate, Milk Chocolate, & Yogurt Covered cranberries, Net Wt. 5 oz (140g) Packaged under the following names:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cape Cod Provisions LLC
FDA (openFDA food enforcement)
Reported Feb 24, 2016
Pint Umpqua Dairy Cultured Sour Cream, Item no. 03654, net w. 16 oz.; UPC 0 71203 00403 4. Half Pint Umpqua Dairy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Umpqua Dairy Products Co.
13 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 17, 2016
RadSuite, a picture archive and communications system. Model Numbers Versions 5.30.0, 5.30.1, 5.30.2, 5.30.2 SB0344,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Feb 17, 2016
Zzang! Original Candy Bar, 2.5 oz., packaged in preprinted cardboard boxes, UPC 8 44397 00014 0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zingerman's Candy Manufactory
4 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 10, 2016
ACIST Medical Systems, BT2000 Automated Manifold Kit (SKU 014613) and CPT2000 (SKU 014623) Automated Manifold Kits,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acist Medical Systems
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
The ABX PENTRA Cholesterol CP ref. A11A01634 is an in vitro diagnostic assay for quantitative determination of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 10, 2016
Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily used as non-invasive homecare devices, for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Resmed Corporation
FDA (openFDA device enforcement)
Reported Feb 3, 2016
EliA SmDP Well, Article Number 14-5624-01 Product Usage: EliA SmDP is intended for the in vitro semi-quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia Ab
FDA (openFDA device enforcement)
Reported Jan 20, 2016
Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Skytron, Div. The KMW Group, Inc.
FDA (openFDA device enforcement)
Reported Jan 13, 2016
Software version VD10E for Syngo X-Workplace; Picture archiving and communication system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, 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.