FDA Device recall Z-1556-2015
CareFusion Vital Signs LightWand Stylet
- FDA Device
- Class II
- terminated
- Published 2015-05-06
On 2015-05-06 the FDA classified a Class II recall of CareFusion Vital Signs LightWand Stylet by Vital Signs Colorado, citing 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 ster….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1556-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-13 |
| Published | 2015-05-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Vital Signs Colorado |
| Distribution | US |
Product
CareFusion Vital Signs LightWand Stylet. A device inserted into an endotracheal tube to aid in the intubation procedure.
Reason
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.
Identifiers
| code_info | Catalog Number 3910 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1556-2015%22
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