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 Jun 13, 2018
Restoris MCK Onlay Insert Extractor.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gyrus Acmi, Incorporated
FDA (openFDA device enforcement)
Reported Jun 6, 2018
CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maquet Datascope Corp. - Cardiac Assist Division
FDA (openFDA device enforcement)
Reported Jun 6, 2018
VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June 2017 equipped with keypads with Ref.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet SAS
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable (6 Towels per Pack) / product # AVID266 Sterile This…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries Inc.
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Heinens Organic Nut Mix Net Wt. 9 oz (255g) Distributed By Heinens, Warrensville Hts., OH 44128 UPC 0-36232-01871-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ohio Hickory Harvest Brand Products Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 6, 2018
LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torax Medical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
Edwards Lifesciences' IntraClude Intra-Aortic Occlusion Device. Packaged in a sterile barrier system. Model Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 30, 2018
Southwestern Gourmet Butter Popcorn Grand Canyon Foods, Phoenix, AZ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Grand Canyon Foods International LLC.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 30, 2018
ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U, Rx, Sterile. Incorrect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
smith&nephew 5o (5 degree) GENESIS(R) II VALGUS BUSHING, REF CATALOG NUMBER 71440014 The GENESIS II Knee System…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
AMENDIA Omega Lumbar Interbody Fusion Device, Part Number 72-00-2-092812-11 The OmegaLIF(TM) (LIF(TM)) Expandable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spinal Elements
FDA (openFDA device enforcement)
Reported May 23, 2018
Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott
FDA (openFDA device enforcement)
Reported May 23, 2018
DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured and Distributed by eBars, LLC, Franklin, TN 37064…
High riskUsing this product could cause serious injury, illness or death — stop using it now.eBars
12 more products in this recall
FDA (openFDA food enforcement)
Reported May 23, 2018
Tosoh ST AIA-PACK HbA1c, HbA1c Reagent, Pt. No. 025218 The device is designed for In Vitro Diagnostic Use Only for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 23, 2018
Vans gluten free Original 6 WAFFLES NET WT 9 OZ (255g) INGREDIENTS:***VAN'S GLUTEN FREE MIX (BROWN RICE FLOUR, POTATO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Tyson Foods Discovery Center
FDA (openFDA food enforcement)
Reported May 23, 2018
Persona Stemmed Tibial Provisional Size H Left, Item Number 42532108301 For use during orthopaedic surgery for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported May 16, 2018
LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Shoulder Set is intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
FDA (openFDA device enforcement)
Reported May 16, 2018
Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger Medical, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported May 16, 2018
Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz (84g); UPC: 853787005368
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Munk Pack Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 16, 2018
Soozie s Doozies Sugar Cinnamon Snickerdoodle Cookie Dough, 16 ounce, plastic pouch, 6 pouches per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.National Foodworks Services
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.