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 Dec 21, 2016

Roasted & Salted Sunflower Kernels under the following brand names: AMISH FARMS SALEM, OHIO 44460 5.5 oz plastic bag…

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

Ohio Hickory Harvest Brand Products Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 21, 2016

Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm (EMS) The system is intended for use in surgical…

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

Steris Corporation

FDA (openFDA device enforcement)

Food

Reported Dec 21, 2016

Trader Joe's Mediterranean Hummus SKU #90642

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

Two Chefs On A Roll, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 14, 2016

A&W Cream Soda, 20 FL OZ, Caffeine Free

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

Chesterman Co.

FDA (openFDA food enforcement)

Food

Reported Dec 14, 2016

Cookie Dough Ice Cream packed under the following brand names and sizes: 1. Chocolate Shoppe Ice Cream Company, 3…

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

Chocolate Shoppe Ice Cream Co., Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2016

Empowr Knee System Product Usage: Non-porous proximal tibial baseplate implants, utilized in either posterior cruciate…

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

Encore Medical, LP

FDA (openFDA device enforcement)

Food

Reported Dec 14, 2016

McConnell's Fine Ice Cream Dutchman's Chocolate

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

McConnell's Ice Cream, Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 14, 2016

Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA Analytical X-Ray System

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

Olympus Scientific Solutions Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2016

Brilliance 64 728231 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by…

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

Philips Medical Systems (Cleveland) Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 14, 2016

ADVIA 560 Hematology Systems, Siemens Material Number (SMN) 11170842, IVD.

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2016

ConforMIS iTotal Cruciate Retaining (CR) Knee Replacement System, Sterile Catalog Number: TCR-111-1111. Intended for…

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

ConforMIS, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2016

Monaco RTP System; Used to make treatment plans for patients with prescriptions for external beam radiation therapy.

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

Elekta, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 7, 2016

MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche OMNI S Analyzer: cobas b 221<6>Roche OMNI S6 system The Roche…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2016

COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…

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

AtriCure, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 30, 2016

BM Westco Mster Mix Raised Donut Mix, 50#

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

CSM Bakery Products NA

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2016

Access Ostase Calibrators, Catalog No. 37305, B83876 Product Usage: The Access Ostase Calibrators are intended to…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2016

Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and…

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

McCain Foods USA

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2016

Brilliance iCT Computed Tomography X-ray system, Model 728306

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

Philips Medical Systems (Cleveland) Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2016

Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2016

RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2016

On Lid: Turkey Hill, Rocky Road, 48 FL. OZ.. In small letters at the top of the lid reads: "Dutch Chocolate ice cream…

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

Turkey Hill Dairy, LP

FDA (openFDA food enforcement)

Meat & poultry

Reported Nov 17, 2016

La Quercia Retira Productos De Cerdo Seco Por No Estar Suficientemente Deshidratados

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

La Quercia Operating LLC

USDA FSIS

Food

Reported Nov 16, 2016

Dorothy Lynch Homestyle 8 oz., 16 oz., and 32 oz. bottles (12/case) and 128 oz. bottles (4/case)

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

Tasty Toppings Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 16, 2016

Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…

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

Zimmer Surgical Inc.

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.