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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.

Medical devices

Reported Jan 13, 2016

Natus Quantum System with NeuroWorks Software. Catalog /Part Numbers: 013926. The Natus Quantum Amplifier is intended…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Natus Neurology dba Excel Tech., Ltd. (XLTEK)

FDA (openFDA device enforcement)

Medical devices

Reported Jan 13, 2016

Software version VD10E for Syngo X-Workplace; Picture archiving and communication system.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

Radiographic Transparency for Certain and External Connection Tapered Implants. Images that assist with measurements…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet 3i, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Trumpf Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Vancomycin Screen Agar

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Biomerieux

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

MicroCutter Xchange 30 Blue Cartridge, FG-025320; The MicroCutter XCHANGE 30 Blue Cartridge and MicroCutter XCHANGE 30…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardica, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Aegis Torque Handle CATALOG NO. : 2871-10-800. A spinal surgical instrument used on the AEGIS Anterior Lumbar Plate…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DePuy Spine, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Hook Blade, Angled. Part number 7058A. Sterile disposable blade for use with Endoscopic Tarsal Tunnel Decompression…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Instratek, Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Reagent Management System (RMS) Dimension EXL with LM Product Usage: The Reagent Management System (RMS) is a module…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Double Trigger Handpiece. Rx only Made in Switzerland

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 23, 2015

Del Pasado Dice Green Chiles 100% Fire Roasted and Peeled NET WT. 6 LB 3 OZ (2.81 kg) packaged in #10 steel cans

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bruce Foods Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Dec 23, 2015

MOSAIQ Oncology Information System. Used to manage workflows for treatment planning and delivery.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

Fujifilm Medical Systems Duodenoscope, Model Numbers ED-200XU, ED-200XT, ED-250XT, ED-310XU, ED-420XL, ED-410XT,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fujifilm Medical Systems U.S.A., Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 23, 2015

Sprinkle King, Lime Green Sanding Sugar, 30611201.00N, UPC #30763089281012, NET WT: 150 lb (68.182 kg)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kerry Foods

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 23, 2015

Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Myco Medical Supplies Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 16, 2015

RBT, Internal Implant, Laser-Lok, 5.0 x 15mm, 5.7 Platform, REF LPBR5015, Rx only, Sterile R, BIOHORIZONS(R), Dental…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioHorizons Implant Systems Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2015

1.) Essential EVERYDAY Chocolate Flavored Dairy Whipped Topping, Made with Real Cream, Ultra-Pasteurized Grade A, NET…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Saputo Dairy Foods USA, LLC

FDA (openFDA food enforcement)

Food

Reported Dec 16, 2015

Kroger 100% natural apple FROM CONCENTRATE 64FL OZ. INGREDIENTS: APPLE JUICE FROM CONCENTRATE (FILTERED WATER, APPLE…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 16, 2015

Valeant Pharmaceuticals North America Model No. Spag-2 Small Particle Size Aerosol Generator SPAG-2 6000 is a pneumatic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Valeant Pharmaceuticals North America LLC

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.