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.
3,919 stored notices name Colorado, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Colorado too — those are in the archive.
Reported Apr 9, 2014
Weck Vista Universal Laparoscopic Port, Size 5/10mm x 100mm, Catalog No. 405910, Weck Vista Universal Laparoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 2, 2014
Siemens Artis Q and Artis Q biplane systems Product Usage: Interventional Fluoroscopic X-ray
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 2, 2014
Drill Template and the Saw Guide for the Ulna Osteotomy System. Intended for fixation of fractures, osteotomies,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes, Inc.
FDA (openFDA device enforcement)
Reported Apr 2, 2014
HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed grafts (EU) Product Usage:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Thoratec Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 2, 2014
DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Velocity Medical Solutions, LLC
FDA (openFDA device enforcement)
Reported Apr 1, 2014
Oklahoma Firm Recalls Chicken Products Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.AdvancePierre Foods, Inc.
USDA FSIS
Reported Mar 26, 2014
Reusable Clip Applier Manufactured by AtriCure, Inc., 6217 Centre Park Drive, West Chester, OH 45069. The Reusable Clip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atricure Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens, FL 33410 USA 1-800-342-5454***EDAZ , EDAZx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 26, 2014
GE Healthcare Optima CT580/Discovery CT590RT scanners running software version 13BW16.3. The Discovery CT 590 RT and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Mar 26, 2014
High Mowing Organic Sprouting Seeds Ancient Eastern Blend , 4 oz. resealable plastic bag UPC Code: 872724005445
Moderate riskThis product could cause temporary or reversible health problems — stop using it.High Mowing Organic Seed
FDA (openFDA food enforcement)
Reported Mar 26, 2014
Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. The HeartStart FR3 is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems North America Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 26, 2014
2.5MM Aggressive Blade Known as a Sinuscopic Shaver Blade, this device is composed of a metal cutter and plastic drive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Mar 26, 2014
FLOUR TORTILLAS: FAJITA 6" 15 0Z UPC Code 1569602222, HOMESTYLE 8" 24 OZ UPC Code 1569602221, BURRITO 10" 28OZ UPC Code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tortillas Mexico Mexico, Incorporated
2 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 26, 2014
Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 PAT N-K FLEX MBACK SZ 1 PAT N-K FLEX MBACK SZ 2 PAT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
bioMerieux PREVI Isola System (General purpose,microbiology, diagnostic Medical Device), (REF 29500/29500R),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
Navigator Surgical Kit Product Usage: Molded plastic tray used in holding various dental instruments for autoclave…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
Jalapeno Ground 40, Elite Spice Code #JP9520, 50 lb poly-lined cartons labeled in part ***Elite Spice Inc. 7151…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Elite Spice Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 19, 2014
GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, Innova 3131IQ;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
HER2 Image Analysis Manual Read of HER2 Digital Slides ER/PR Image Analysis IHC PR Breast Tissue Manual Read of Digital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Imaging, Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
Classic Sysco Custom Ready to Use Cherry Pie Filling; with other Natural Flavors #10 can - Net wt 7 lbs (3.18kg) UPC 1…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lyons Magnus
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 19, 2014
Smith & Nephew RENASYS Soft Port REF: 66800799 (The RENASYS Soft Port Dressing Kits are used in conjunction with…
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 Mar 19, 2014
4040-2: Umbilical 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
12 more products in this recall
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.