Recalls distributed in Colorado
These notices name Colorado 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.
3,918 stored notices name Colorado, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Colorado too — those are in the archive.
Reported Feb 22, 2017
BrightView XCT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 22, 2017
LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2017
AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Empowr PS Knee Tibial Insert; Model 343-14-709 The EMPOWR PS tibial insert are made from Highly Cross-Linked Vitamin E…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Bariatric Bed - BAR600IVC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Feb 15, 2017
DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Dannon Company, Inc.
FDA (openFDA food enforcement)
Reported Feb 15, 2017
Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
FDA (openFDA drug enforcement)
Reported Feb 8, 2017
Olympus Scientific Solutions Americas Corporation ( OSSA ) VANTA¿ XRF Analyzer. Model Vanta VCR and Vanta VMR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Scientific Solutions Americas
FDA (openFDA device enforcement)
Reported Feb 8, 2017
Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy strawberries & cream ice cream, NET WT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 1, 2017
FRONT: Stauffer's Animal Crackers Original; Net Wt. 32 OZ.; BACK: (best by date): 07SEP17; (bag lot numbers) LC120716…
High riskUsing this product could cause serious injury, illness or death — stop using it now.D. F. Stauffer Biscuit Co., Inc.
FDA (openFDA food enforcement)
Reported Feb 1, 2017
Hitachi Oasis MRI System - C-Spine Coil
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Mallinckrodt Pharmaceuticals INOmax DSIR Plus delivery system. Model 10007. Delivers INOMAX (nitric oxide for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INO Therapeutics (dba Ikaria)
FDA (openFDA device enforcement)
Reported Feb 1, 2017
SCC Soft Computer Softbank II software Product Usage: Supports single and multi-site transfusion services in healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soft Computer Consultants, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Atlas Meat Company Recalls Pork Products Due To Misbranding
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Atlas Meat Company
USDA FSIS
Reported Jan 25, 2017
Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dicom Grid Inc.
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Monaco RTP System. Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Novation Cemented Plus Femoral Stem, 12/14, Collared, Standard Offset, Matte, Cemented, Size 15.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Medacta International SA, M.U.S.T. Rod, REF 03.50.433, Size 5.5mm, Length 480mm, Type Straight, Mat Co-Cr-Mo The rods…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medacta USA Inc.
FDA (openFDA device enforcement)
Reported Jan 25, 2017
PREMIER EHEC and PREMIER EHEC Bulk.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
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Other states
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.