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Vital Signs Colorado Inc. recalls CareFusion Vital Signs LightWand Stylet. A device inserted into an endotracheal tube to aid in the intubation procedu
Recalled May 6, 2015 · FDA recall Z-1556-2015 · Vital Signs Colorado
Hazard
Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand Stylet catalog numbers 3910 and 3960 due to a potential patient safety risk involving a breach in the sterile packaging that may not be recognized prior to use. · FDA Class II
Units
82,820
Sold at
Worldwide Distribution. US Nationwide, Australia, Canada, Chile, Colombia, Dominican Republic, Ecuador, Egypt, Germany, Guatemala, Hong Kong, India, Israel, Italy, Japan, South Korea, Lebanon, Mexico, Netherlands, New Zealand, Panama, Peru, Poland, Russia, Slovenia, Turkey, United Kingdom, and Qatar.
Description
Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand Stylet catalog numbers 3910 and 3960 due to a potential patient safety risk involving a breach in the sterile packaging that may not be recognized prior to use.
Product
CareFusion Vital Signs LightWand Stylet. A device inserted into an endotracheal tube to aid in the intubation procedure.
Manufacturer(s)
Vital Signs Colorado Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →