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 Oct 31, 2018

BACT/ALERT VIRTUO system, A Unit, with Version R2.0 Firmware Product Usage: The BacT/ALERT VIRTU Microbial Detection…

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

bioMerieux, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

Boston Scientific Maestro 4000 Cardiac Ablation System, Firmware Version 5.14, Model Numbers: M00440000, M0044000D0,…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

J-Plasma Precise 360, single use, disposable. The Bovie J-Plasma Precise 360 Handpiece is used for the delivery of…

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

Bovie Medical Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 31, 2018

Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET WT. 35 OZ (980 g) Callie's Charleston Biscuits; 1895 Avenue…

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

Callie's Charleston Biscuits

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 31, 2018

Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modality that produces…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 31, 2018

Cedar's Chickpea Salad, packaged in an 8oz plastic container, UPC: 044115337767. Product is refrigerated.

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

Cedar's Mediterranean Foods, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 31, 2018

Mitek Screw and Washer Depth Gauge, Product Code 219024

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

DePuy Mitek, Inc., a Johnson & Johnson Co.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

Instrument Arm Drape (Box of 20) individually sealed in poly-Tyvek pouches / Rx Sterile / to used exclusively on the…

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

Ecolab Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

GE Healthcare, Discovery 3.0T MR750, 5148810-2, 5373011-2, 5499460-2.

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

GE Medical Systems, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

O-arm 1000 2nd Edition Imaging System, OARM ASSY Bl70000027 SYSTEM PRODUCT, Model Number Bl70000027 Product Usage: The…

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

Medtronic Navigation, Inc.-Littleton

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2018

APTIO INPUT/OUTPUT MODULE

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

Siemens Healthcare Diagnostics, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…

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

GE Medical Systems, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 24, 2018

La Mexicana Hot Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 128 oz. Gourmet Style Hot Salsa 16 oz.

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

La Mexicana LLC

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 24, 2018

Mindray BeneVision Distributed Monitoring System (DMS), Part No. 115-034413-00

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

Mindray DS USA, Inc. dba Mindray North America

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF:…

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

OriGen Biomedical, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System, Catalog#: 801188

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

Terumo Cardiovascular Systems Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood…

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

Thoratec Switzerland GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2018

Affixus Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180 Product Usage: Intended for the fixation of fractures

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

Zimmer Biomet, Inc.

47 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Oct 19, 2018

GHSW, LLC Recalls Salad Products Due To Possible Salmonella And Listeria monocytogenes Contamination In Corn

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

F&S Fresh Foods

USDA FSIS

Meat & poultry

Reported Oct 19, 2018

SK Food Group Recalls Chicken Products due to Possible Salmonella and Listeria monocytogenes Contamination in Vegetables

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

SK Food Group

USDA FSIS

Medical devices

Reported Oct 17, 2018

Codan Filter (Codan catalog number BC 693) used with Medrad Patient Administration Sets (PAS) and Intego PET Infusion…

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

Bayer Medical Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2018

Colpo-Pneumo Occluder, Part CPO-6

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2018

NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,…

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

Neomed Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 17, 2018

Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product; Net Wt. 70 G/Cookie; Contains: Flour, eggs, Baking Soda,…

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

Sarap Asian Fusion

3 more products in this recall

FDA (openFDA food 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.