FDA Device recall Z-2951-2020
SICAT IMPLANT V2.0
- FDA Device
- Class II
- terminated
- Published 2020-09-16
On 2020-09-16 the FDA classified a Class II recall of SICAT IMPLANT V2.0 by Sicat And Kg, citing A dentist found implant positions are not correctly exported from the implant planning software SICAT IMPLANT V2.0 - for the specific export format CMG.DXD.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2951-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-07-15 |
| Published | 2020-09-16 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Sicat And Kg |
| Distribution | n/a |
Product
SICAT IMPLANT V2.0
Reason
A dentist found implant positions are not correctly exported from the implant planning software SICAT IMPLANT V2.0 - for the specific export format CMG.DXD.
Identifiers
| code_info | V2.0 |
|---|
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-2951-2020%22
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