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.
Reported Jan 25, 2017
Delizza Patisserie, Belgian Custard Cream Mini Eclairs, Net Wt. 420g 14.8 oz., UPC Code: 6 76670 00106 9(30 count)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Poppie International Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 25, 2017
Starkey Spring Water, 16.9 FL oz. (500 mL) glass bottle. packed 15 bottles in cardboard box. Product UPC 8 11904 02000…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Starkey Water
FDA (openFDA food enforcement)
Reported Jan 25, 2017
Dark Chocolate Dolcini, In clear plastic cup, 72 individual servings, Store frozen
High riskUsing this product could cause serious injury, illness or death — stop using it now.Steven Roberts Originals, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
Biscuits & Gravy Seasoning CR/ Barrel O' Fun. Product Code: T3669. 50 lb bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.All American Seasonings, Inc.
25 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brand Castle LLC
FDA (openFDA food enforcement)
Reported Jan 18, 2017
Country Gardens Cuisine, Singles, Broccoli Cheese Soup with Rice, Net Wt. 1.25 oz (35 grams)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Copperleaf Kitchen, LLC Comfort Foods Division
FDA (openFDA food enforcement)
Reported Jan 18, 2017
OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 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.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Biograph mCT S(40)-3R, Material Number 10248668 The Siemens Biograph mCT and Biograph mCT Flow systems are combined…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Starkey Spring Water, Item code STC.5, 16.9 FL oz. (500 mL) glass bottle. Product UPC 8 11904 02000 7. Case UPC 8 11904…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Starkey Water
FDA (openFDA food enforcement)
Reported Jan 18, 2017
Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 11, 2017
Ashby's Sterling Peanut Butter Landslide Ice Cream, 3 gallon container, frozen
High riskUsing this product could cause serious injury, illness or death — stop using it now.House Of Flavors, Inc.
FDA (openFDA food enforcement)
Reported Jan 7, 2017
FSIS Issues Public Health Alert For Chicken Strips Products Due To Possible Listeria Contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported Jan 4, 2017
INOVA (benzoyl peroxide) 4%, Easy Pad (tocopherol) 5%, For topical use only, packaged in a box containing: 30 pads of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cipher Pharmaceuticals US LLC
FDA (openFDA drug enforcement)
Reported Jan 4, 2017
Innova 2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Specimen Gate Laboratory 5002-0180, Specimen Gate eReports 5002-0370, Software Version 1.0 Specimen Gate Laboratory is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Health Sciences, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Limu Poke is fresh refrigerated product, distributed in bulk kit, net wt. 4.35 lbs. Each kit includes five individually…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Western United Fish Company, Inc.
FDA (openFDA food enforcement)
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Merge OrthoCase software. The firm name on the label is Merge Healthcare, Hartland, WI.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit; Algovita Spinal Cord…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nuvectra
FDA (openFDA device enforcement)
Reported Dec 28, 2016
DELFIA hFSH kit. In Vitro Diagnostic for the determination of hFSH in serum
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.PerkinElmer Health Sciences, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Apple Orchard Crisp Apple Hard Cider Three packages sizes: ¿ Loose case = 24 12 oz bottles ¿ 12 pack = 12 12 oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Samuel Adams Brewery Co.
FDA (openFDA food 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.