Class II — SICAT GMBH & CO. KG
| Recalling firm | SICAT GMBH & CO. KG |
|---|---|
| Registered facility | SICAT GMBH & CO. KG (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| 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. |
| Product | SICAT IMPLANT V2.0 |
| Quantity | 853 units |
| Distribution | Worldwide distribution |
| Initiated | 2020-07-15 |
| Classified | 2020-09-10 |
| Terminated | 2024-01-03 |
| Recall number | Z-2951-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — SICAT GMBH & CO. KG (Z-2951-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/86165/
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