FDA Device recall Z-2092-2019
ClubMax Laser Projection Series
- FDA Device
- Class II
- ongoing
- Published 2019-08-14
On 2019-08-14 the FDA classified a Class II recall of ClubMax Laser Projection Series by Gk Photonics, citing the User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2092-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-07-10 |
| Published | 2019-08-14 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Gk Photonics |
| Distribution | n/a |
Product
ClubMax Laser Projection Series
Reason
The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.
Identifiers
| code_info | ClubMax Laser Projection Series |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2092-2019%22
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