All recall categories

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.

Food

Reported Nov 28, 2018

Signature Select Mexican Style Roasted Corn; 12 oz.; 12/12oz. units per case; Keep Frozen Until Ready To Use; UPC…

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

Harvest Food Group

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 28, 2018

Irrisept OR, Finished Bottle Assembly 450 ml STEP 1

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

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

3.2mm Proximal Reamer/Cannulated Drill provided as part of the Fibulock Fibular Nail System Pack. FibuLock Nail…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System

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

GE Healthcare, LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro…

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

Luminex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 21, 2018

The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option

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

Stryker Medical Division

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 21, 2018

simple truth organic Red Quinoa Ingredients: organic red quinoa Distributed by The Kroger Co, Cincinnati, OH…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

The Kroger Co.

FDA (openFDA food enforcement)

Food

Reported Nov 21, 2018

Chef Sensations Fire Roasted 1/2" diced onion/pepper blend Net Wt 20 lbs

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

The Wornick Company

FDA (openFDA food enforcement)

Medical devices

Reported Nov 21, 2018

Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of…

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

Zimmer Biomet, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN (BD Nexiva Catheter), Catalog Number 383539 Product Usage:…

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

Becton Dickinson & Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

Centricity PACS-IW with Universal Viewer version 5.0.x with PACS-IW foundation displays medical images (including…

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

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product…

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

Integrity Implants Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

TB Series Bipolar Pacing Leads, French Size 4F, 5F, 6F for Curve Type Straight, Atrial J, 60 degree Curve, and Right…

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

Oscor, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2018

R&D systems, a bio-techne brand Human Total 25-OH Vitamin D IVD ELISA Kit, REF RDKAP1971

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

R & D Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

EXACTAMIX Empty EVA Bags - 250 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be…

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

Baxter Healthcare Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

BD Max Instrument Reader Spare Part, Catalog Number 8090369/443364, 44336409 (Repaired Reader spare part) - Product…

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 Nov 7, 2018

Zilver 518 Biliary Stent 4mm x 20mm, Catalog Number: ZIB5-125-4.0-20 Product Usage: The Zilver 518 and 635 Biliary…

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

Cook Medical Incorporated

38 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 7, 2018

feel good foods VEGETABLE FRIED RICE NET WT 9 OZ (255G), UPC: 8 99039 00212 9. Frozen.

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

Feel Good Foods Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 7, 2018

Foodstirs Modern Baking; Organic Minute Mug Cake Mix Celebration Confetti - 4 - 2.54 oz. (72g) Pouches per carton…

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

Foodstirs

FDA (openFDA food enforcement)

Food

Reported Nov 7, 2018

Forager Project Organic Protein Plant Shake Nuts & Vanilla 12 fl oz. UPC: 8 14558 02038 6

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

Forager Project LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 7, 2018

Hoffman LRF Hexapod Strut, Extra Short 89mm-109mm, Model Number 4935-0-010. Product Usage - The Hoffmann LRF System is…

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

Stryker GmbH

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 7, 2018

EBI Osteogen Implantable Bone Growth Stimulator The OsteoGen Implantable Bone Growth Stimulator is indicated in the…

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

Zimmer Biomet, Inc.

1 more product in this recall

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.