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.
3,863 stored notices name Colorado, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Colorado too — those are in the archive.
Reported May 22, 2013
Proplege Coronary Sinus Catheter model PR9, 11 French Introducer, kitted with PR9. Product Usage: The catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported May 22, 2013
GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported May 22, 2013
Heartland Gourmet Gluten Free double chocolate cookie mix, DAIRY FREE, packaged in 16-oz. boxes. Manufactured by:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartland Gourmet, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 22, 2013
Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heartware Inc.
FDA (openFDA device enforcement)
Reported May 22, 2013
1-DAY ACUVUE MOIST Brand Contact Lenses, soft disposable contact lenses. The Vistakon (etafilcon A) Soft (hydrophilic)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Vision Care, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 15, 2013
ExoShape Soft Tissue Fastener 12 mm x 30 mm REF 1101-00-1230. For use in the fixation of ligaments, tendons or soft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medshape Solutions, Inc.
FDA (openFDA device enforcement)
Reported May 15, 2013
Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage: Designed for use in a medical facility under…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus America Inc.
FDA (openFDA device enforcement)
Reported May 15, 2013
Wallace Sure-Pro/ Sure-Pro Ultra Embryo Replacement Catheters (with ultrasound) Product Code: PE623 Sure-Pro¿ Embryo…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 15, 2013
Codman(R) Collins Radioparent Sternal Blade Nylon,4 3/4" (121 mm) long, 3" (76 mm) wide, 1 1/2" (38 mm) deep, REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Symmetry Medical/SSI
FDA (openFDA device enforcement)
Reported May 8, 2013
STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
FDA (openFDA device enforcement)
Reported May 8, 2013
BUFFALO TRACE BOURBON FLAVORED CARAMEL SAUCE 8 oz glass jars Net Wt. 8 fl. oz./227 g, PRODUCED BY: APPLECREEK ORCHARDS…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Buffalo Trace Distillery
4 more products in this recall
FDA (openFDA food enforcement)
Reported May 8, 2013
SL3 SOFT-TISSUE Laser (Model LR2002); Manuf: Discus Dental, LLC, 8550 Higuera Street, Culver City CA 90232. The SL3 is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Discus Dental LLC
FDA (openFDA device enforcement)
Reported May 8, 2013
GE, VCT for Discovery VCT, Discovery RX VCT, and Discovery PET/CT 690, Lightspeed VCT, Discovery CT750HD. Intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 8, 2013
Newport Medical Instruments HT70 and HT70 Plus ventilator Power Pac batteries Model number: HT70 and HT70 Plus. The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Newport Medical Instruments Inc.
FDA (openFDA device enforcement)
Reported May 8, 2013
Stryker Howmedica Osteonics Corp. AxSOS System Instrument. The AxSOS Locking Plate System is designed to treat…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported May 1, 2013
all One Active Senior Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters
Moderate riskThis product could cause temporary or reversible health problems — stop using it.All One, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 1, 2013
TriMix Standartd (PGE Stock Sol'n) Injectable Balanced Solutions, Compounding Pharmacy a division of Axium Healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Axium Healthcare Pharmacy dba Balanced Solutions Compounding
25 more products in this recall
FDA (openFDA drug enforcement)
Reported Apr 24, 2013
ACIST Medical Systems Inc. The ACIST Angiographic Injection System is intended to be used for the controlled infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acist Medical Systems
FDA (openFDA device enforcement)
Reported Apr 24, 2013
EVOTECH Endoscope Cleaner & Reprocessor System, P/N 50004 Designed to automatically clean and high-level disinfect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2013
EphBurn 25, 90 count bottle with red capsules
High riskUsing this product could cause serious injury, illness or death — stop using it now.Brand New Energy, LLC
FDA (openFDA food enforcement)
Reported Apr 24, 2013
Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators; BE 183-SUR and BE 183 SUR-12 Manual Jet…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Industries Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Metal cans; labeled as containing 29 oz of pinto beans packed in water and salt
Moderate riskThis product could cause temporary or reversible health problems — stop using it.La Preferida Inc.
FDA (openFDA food enforcement)
Reported Apr 24, 2013
Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device is used as an in vitro diagnostic product.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Siemens syngo WorkFlow SLR, Radiological Information System, Version VA31A SP1/SP2/SP3 The information system syngo(R)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, 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.