FDA Device recall Z-0988-2015
Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries
- FDA Device
- Class II
- terminated
- Published 2015-01-21
On 2015-01-21 the FDA classified a Class II recall of Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries by Ziemer Usa, citing the devices were not shipped with the Starter Kits.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0988-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-18 |
| Published | 2015-01-21 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Ziemer Usa |
| Distribution | US |
Product
Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.
Reason
The devices were not shipped with the Starter Kits.
Identifiers
| code_info | Serial Numbers: FLM4184, FLM2003, FLM3324, FLM1409, FLM2906, FLM2136, FLM4948, FLM3134, FLM4587, FLM3281, FLM2179, FLM1…Serial Numbers: FLM4184, FLM2003, FLM3324, FLM1409, FLM2906, FLM2136, FLM4948, FLM3134, FLM4587, FLM3281, FLM2179, FLM1467, FLM1239, FLM3361, FLM3319, FLM3685, FLM2915, FLM1230, FLM3229, FLM4094, FLM4135, FLM4545, FLM4905, FLM3913, FLM1680, FLM1776 |
|---|
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-0988-2015%22
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