FDA Device recall Z-0992-2015
Infinite 200PRO The Tecan Infinite 200 is a multifunctional microplate reader with injector option
- FDA Device
- Class III
- terminated
- Published 2015-01-21
On 2015-01-21 the FDA classified a Class III recall of Infinite 200PRO The Tecan Infinite 200 is a multifunctional microplate reader with injector option by Tecan Us, citing incorrect lumi firmware version installed (E.027 instead of V2.00).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0992-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-11-10 |
| Published | 2015-01-21 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Tecan Us |
| Distribution | MD |
Product
Infinite 200PRO The Tecan Infinite 200 is a multifunctional microplate reader with injector option. The Infinite 200 provides high performance for the vast majority of todays microplate applications and research and is robotic compatible. The infinite 200 has been designed as a general purpose laboratory instrument for professional use, supporting common 6 to 384-well microplates conforming to the ANSI/SBS standards.
Reason
Incorrect lumi firmware version installed (E.027 instead of V2.00)
Identifiers
| code_info | Material number: 30050303, Lot numbers: 1010005108, 1012003953, 1108005760, 1306007560 and 1311008591. |
|---|
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-0992-2015%22
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