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 Jan 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abdallah Candies, Inc.
FDA (openFDA food enforcement)
Reported Jan 7, 2015
Hypodermic Needle Pro¿ Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Needle Pro¿ Edge Safety…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed by Kimberly Clark Global Sales, LLC.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Halyard Health
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
DPM 6 Patient Monitor and DPM 7 Patient Monitor. The product affected is the Mindray IBP module, P/N is 6800-30-50485…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Dec 31, 2014
Private Selection Extreme Moose Tracks Ice Cream; packaged in plastic 48 fl oz containers, UPC Code: 11110-00456
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
FDA (openFDA food enforcement)
Reported Dec 24, 2014
ASTS-LG1212: Anterior Lumbar Interbody Fusion Spine Truss System (orthopedic implant) Large, 12 degrees lordosis, 12 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.4-Web Inc.
FDA (openFDA device enforcement)
Reported Dec 24, 2014
Turbo Troponin I For in vitro diagnostic use for the quantitative measurement of troponin I in serum, heparinized or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT) and integrates with an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snug Seat Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Amerigel Hydrogel Wound Dressing Wound management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 or 4 Bottle(s) (6.6 mL/27.0 mL) anti-T3 (sheep) coated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Synthes Titanium Polyaxial Reduction Head for Titanium Matrix Spine Screws: The Titanium Polyaxial Reduction Head is a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Edwards Lifesciences Vent Catheters, . Packaged sterile and non-pyrogenic in a sealed, peel-type pouch. Model Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 26, 2014
Transport Chair and Rollator in 1, Model HE21630011 Burgundy and HE21630011 Blue. This is a walker/rolling chair. Used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Silver Star Brands
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Prescription eyeglass safety lenses. Vision correction
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eyemart Express Ltd.
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Thyroglobulin (1D4) is a mouse anti-human monoclonal antibody produced as a tissue culture supernatant, and supplied in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Nov 12, 2014
Stryker SmartLife Large Aseptic Housing REF 7126-120-000 Rx Only The SmartLife" Aseptic Housings are designed to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2014
DMI Duro-Med Industries Rollator Transport Chair; Wheel Size: 7 1/4"; Overall Width: 23 1/2"; Seat Height: 21 1/4";…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Briggs Medical Service Company d.b.a. Mabis
FDA (openFDA device enforcement)
Reported Nov 5, 2014
Laksell Gamma Knife Perfexion
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Nov 5, 2014
Family Gourmet Long Grain Enriched White Rice in 32 oz. clear plastic bags (SKU: 1218898) and 80 oz. clear plastic bag…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Family Dollar Stores - NC Distribution Center
FDA (openFDA food enforcement)
Reported Nov 5, 2014
The GemStar Power Supply is an accessory for the GemStar Infusion Pump. It is a two piece assembled switching power…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 5, 2014
ACCU-CHEK Spirit Combo insulin infusion pump sold as part of Accu-Chek Combo System Product Usage: The ACCU-CHEK Combo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, 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.