Vital Signs Colorado Inc.: Medical Device Recall in 2015 - (Recall #: Z-1557-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Introduction Pack. A device inserted into an endotracheal tube to aid in the intubation procedure.

Product Classification:

Class II

Date Initiated: March 13, 2015

Date Posted: May 6, 2015

Recall Number: Z-1557-2015

Event ID: 70753

Reason for Recall:

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.

Status: Terminated

Product Quantity: 399

Code Information:

Catalog Number 3960

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated