Vital Signs Colorado Inc.

Complete recall history across all FDA and CPSC categories — 4 total recalls

Vital Signs Colorado Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (4)

FDA medical device enforcement actions by Vital Signs Colorado Inc.

Date Product Reason Class
Mar 13, 2015 CareFusion Vital Signs LightWand Stylet. A device inserted into an endotra... Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand Styl... Class II
Mar 13, 2015 Introduction Pack. A device inserted into an endotracheal tube to aid in the... Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand Styl... Class II
Dec 26, 2013 Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for use... A circuit in use was occluded by a blue port cap that was inadvertently attac... Class II
Aug 17, 2012 Vital Signs Disposable General Purpose 9 French Temperature Probe For monito... There is a potential for epistaxis during use of the Disposable General Purpo... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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