FDA Device recall Z-0169-2015
Elite XPL (Pulsed Light) Handpiece for the Cynosure Elite MPX Laser System
- FDA Device
- Class II
- terminated
- Published 2014-11-12
On 2014-11-12 the FDA classified a Class II recall of Elite XPL (Pulsed Light) Handpiece for the Cynosure Elite MPX Laser System by Cynosure, citing if the laser system is turned on and the user adjusts, installs or removes the XPL pulsed light handpiece, there is a potential risk of an electrical shock.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0169-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-10-09 |
| Published | 2014-11-12 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Cynosure |
| Distribution | US |
Product
Elite XPL (Pulsed Light) Handpiece for the Cynosure Elite MPX Laser System
Reason
If the laser system is turned on and the user adjusts, installs or removes the XPL pulsed light handpiece, there is a potential risk of an electrical shock
Identifiers
| code_info | All Serial numbers |
|---|
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-0169-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.