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 May 3, 2017

ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14.…

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a…

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

Heartware

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported May 3, 2017

Donepezil HCl tablets, 10mg, packaged in 10x10 blister packs per carton (100 Unit Dose) container, Rx only,…

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

Mckesson Packaging Services

FDA (openFDA drug enforcement)

Medical devices

Reported May 3, 2017

Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in…

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

Orthosoft, Inc. dba Zimmer CAS

FDA (openFDA device enforcement)

Medical devices

Reported May 3, 2017

Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood…

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

Remel Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 26, 2017

AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9

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

Advanced Fresh Concepts Corp.

FDA (openFDA food enforcement)

Food

Reported Apr 26, 2017

Asher's Chocolate Co, Milk Chocolate (11481) Pretzel Cluster; Net Wt. 5 lb.; Asher's Chocolate Co, Milk Chocolate…

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

Ashers Chocolates/Lewistown, Inc.

86 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 26, 2017

Software version 4.44A utilized on the BD MAX System

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

Bd Life Sciences

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2017

SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 26, 2017

ChloroFields Micro-greens Asian Mix, Net Wt. 1.5 OZ, packed in clear plastic clamshells

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

ChloroFields

FDA (openFDA food enforcement)

Medical devices

Reported Apr 26, 2017

Hemotherm CE, model 400CE, Heater-Cooling Device

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

Cincinnati Sub-Zero Products Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2017

Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product…

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

Covidien Medtronic

FDA (openFDA device enforcement)

Medical devices

Reported Apr 26, 2017

PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes…

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

CP Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 26, 2017

Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # PBP201 - 10-1.2 oz. packets;…

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

Nutiva

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 26, 2017

Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

VIDAS Estradiol II, Ref 30431-01, 60 tests The VIDAS Estradiol II (E2 II) assay is intended for use on the instruments…

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

BioMerieux SA

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

ViperWire Advance Peripheral Guide Wire with Flex Tip, Model No. VPR-GW-FT18. Sterilized with Ethylene Oxide. The guide…

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

Delta, Catalog Number: MS18597 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus.…

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

Draegar Medical Systems, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

da Vinci Xi EndoWrist Suction Irrigator, 8 mm instrument; PN 480299-03; and SOFTWARE, EMBEDDED RLS, IS4000,…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 19, 2017

LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797

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

Nonna Foods

FDA (openFDA food enforcement)

Medical devices

Reported Apr 19, 2017

Specimen Gate Laboratory; Product Number: 5002-0180 Specimen Gate Laboratory is intended for use as a data processing…

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

PerkinElmer Life and Analytical Sciences, Wallac, OY

FDA (openFDA device enforcement)

Drugs

Reported Apr 19, 2017

Estradiol Micronized Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co.,…

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

Qinhuangdao Zizhu Pharmaceutical, Co.

6 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported Apr 19, 2017

Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Apr 19, 2017

CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.

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

Smiths Medical ASD 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.