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.

Medical devices

Reported Mar 15, 2017

Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker Endo-Bronch with Flex Tip). Model Numbers:…

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

Parker Medical

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2017

Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,

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

Remel Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 15, 2017

Trader Joes Imported English Authentic Lemon Curd, 10.5oz (300g), 24 jars/case

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

Trader Joes Company

FDA (openFDA food enforcement)

Medical devices

Reported Mar 15, 2017

Roth Net Polyp Retrieval

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

US Endoscopy Group Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2017

Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general…

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

Villa Sistemi Medicali S.P.A.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

BD AffirM VPIII Microbial Identification Test

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Food

Reported Mar 8, 2017

White Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes

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

Bell Stone Toffee

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 8, 2017

Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…

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

Cook Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

EliA Sample Diluent, Article number, 83-1023-01

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

Phadia US Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2017

Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.

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

Windstone Medical Packaging, Inc.

123 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 1, 2017

AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.

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

Applied Medical Technology Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 1, 2017

Falafel King Tzatziki Sauce. 10 ounce. Plastic container

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

Falafel King Ent, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 1, 2017

N Latex HCY REAGENT, REF/Catalog OPAX03 /SMN 10445973 , IVD Product Usage: In-vitro diagnostic reagents for the…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 1, 2017

Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.

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

Tosoh Bioscience, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 22, 2017

Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20

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

Bwi Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 22, 2017

Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

BrightView XCT

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 22, 2017

CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…

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

Siemens Healthcare Diagnostics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a…

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

AtriCure, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Empowr PS Knee Tibial Insert; Model 343-14-709 The EMPOWR PS tibial insert are made from Highly Cross-Linked Vitamin E…

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

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2017

Bariatric Bed - BAR600IVC

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

Invacare Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new Colorado recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.