SYNTHES GMBH / Synthes Produktions GmbH
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (4)
- SYNTHES GMBH FEI 3009417901 · CH
- Synthes GMBH FEI 3000270450 · CH
- SYNTHES GMBH / Synthes Produktions GmbH FEI 3002807305 · CH
- Innomedic GmbH FEI 3013510178 · DE
Recalls & enforcement
- Class IITerminated2020-06-16One lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a 3 (representing 3mm) when it should have been packaged with body clip etched with a 12 (representing 12mm).
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “SYNTHES GMBH / Synthes Produktions GmbH — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-9071542-synthes-gmbh-synthes-produktions-gmbh/
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