FDA Device recall Z-1178-2019
Olympus Diego Elite Console MDCONS 100
- FDA Device
- Class II
- terminated
- Published 2019-04-24
On 2019-04-24 the FDA classified a Class II recall of Olympus Diego Elite Console MDCONS 100 by Gyrus Acmi, citing olympus Diego Elite Consoles may inadvertently permit activation of the RF energy feature when used with Diego Elite blades.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1178-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-08 |
| Published | 2019-04-24 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Gyrus Acmi |
| Distribution | US |
Product
Olympus Diego Elite Console MDCONS 100
Reason
Olympus Diego Elite Consoles may inadvertently permit activation of the RF energy feature when used with Diego Elite blades
Identifiers
| code_info | Consoles containing software UIC version 2.3.9.0 and RTC version 00.01.23 US Serial Numbers: GB00197 GB02851 GB0438…Consoles containing software UIC version 2.3.9.0 and RTC version 00.01.23 US Serial Numbers: GB00197 GB02851 GB04383 GB00235 GB02878 GB04384 GB00238 GB02995 GB04386 GB00270 GB03000 GB04400 GB00278 GB03054 GB04401 GB00280 GB03171 GB04412 GB00870 GB03173 GB04414 GB00886 GB03201 GB04416 GB00917 GB03232 GB04417 GB00925 GB03431 GB04419 GB00937O GB03519 GB04420 GB00949 GB03675 GB04481 GB02173 GB03714 GB04482 GB02250 GB03717 GB04483 GB02263 GB03733 GB04484 GB02268 GB03746 GB04485 GB02289 GB03782 GB04486 GB02366 GB03790 GB04488 GB02368 GB03791 GB04489 GB02372 GB03793 GB04490 GB02381 GB03923 GB04491 GB02390 GB03941 GB04496 GB02406 GB03961 GB04497 GB02422 GB03966 GB04498 GB02442 GB04008 GB04503 GB02446 GB04022 GB04506 GB02453 GB04035 GB04507 GB02457 GB04041 GB04515 GB02507 GB04195 GB04516 GB02538 GB04212 GB04517 GB02539 GB04214 GB04534 GB02602 GB04241 GB04540 GB02613 GB04243 GB04592 GB02716 GB04 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1178-2019%22
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