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 Aug 15, 2018

Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video…

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 Aug 15, 2018

Modera Modular Pedicle Screw System Shank Insertion Instrument, 3-107-07

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

New Era Orthopaedics, LLC

FDA (openFDA device enforcement)

Food

Reported Aug 15, 2018

Matiz Raw Apricot Bar Demi-luna 8.8 ounces bar, packaged in shrink wrap plastic, UPC 8 32924 00543 0. Product is…

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

Power Selles Imports dba Culinary Collective

FDA (openFDA food enforcement)

Food

Reported Aug 15, 2018

utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 17301, UPC:…

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

Utz Quality Food Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 15, 2018

AirLife Resuscitation Device, Adult labeled as the following: a. Adult, with mask, oxygen reservoir bag, Part Number…

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

Vyaire Medical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…

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

Water Pik, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300;…

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

Cayenne Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Instrument trays used to store AltiVate Small Shell Trials (FA S ALTIVATE RSP HUM TRLS SM). Metal container with lid…

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

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22

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

GE Healthcare, LLC

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to…

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

Integra LifeSciences Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

XLTEK EMU40EX EEG Headbox

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 Aug 8, 2018

Nicolet¿ Ambulatory EEG

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

Natus Neurology Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 8, 2018

Homestyle Seasoned Croutons: 4 oz. foil pouch Item # 73689 UPC 10083661736898 Sugar Foods Corporation 6190 E. Slauson…

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

Sugar Foods Corporation Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…

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

Bard Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well…

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

Bio-Rad Laboratories Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 1, 2018

Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with caramel flavored chips; NET WT; 2 oz. UPC: 0 31535 59962 2…

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

Biscomerica, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

CORAIL Cementless Femoral Stem HA Coated Standard Size 11, Catalog No. 3L92511

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic…

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

GE Medical Systems, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

ImplantDirect, Dental implants intended for use in partially and fully edentulous upper and lower jaws in support of…

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

Implant Direct Sybron Manufacturing, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419,…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Gibco CTS OpTmizer T Cell Expansion Serum Free Medium, bag format, Model Numbers A1048503 and A1022103. Tissue and cell…

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

Life Technologies, Corp.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Nobel Biocare 17¿ Multi-Unit Abutment, Conical Connection NP, 2.5mm, REF 36614. Product Usage: Intended to be used in…

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

Nobel Biocare USA LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

OMNI Hip System, ApeX-LNK Acetabular Inserts 0 degree, 4+mm offset, Product Codes: H6-14436, H6-13928 & H6-14836…

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

OMNIlife science 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.