Femoral and Tibial Cutting Block Adapter Base — Class II medical device recall Z-0959-2017
Terminated recall by Brainlab AG, reported 2017-01-18, distributed in DC, NY, OK, WI. Brainlab Knee Navigation System: Femoral and Tibial Cutting Block Adapter Base with specific serial numbers mi
| Recall number | Z-0959-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Brainlab AG, Munich, Germany |
| Recall initiated | 2016-10-27 |
| Classified | 2017-01-06 |
| Reported by FDA | 2017-01-18 |
| Terminated | 2018-04-11 |
| Distributed | DC, NY, OK, WI |
| Countries outside the US | AE, AU, CH, DE, GB, IN, JP, MY, SG |
| Quantity | 29 units |
| UPC / GTIN / UDI-DI | 04056481002626 |
| Lot numbers | 1267114001, 1267114070, 1308615001, 1308615045 |
| Model numbers | 41866-77A, 41888-04, 99700-43 |
Product
Femoral and Tibial Cutting Block Adapter Base. Brainlab knee, BrainLAB Image Guided Surgery System / Instrument, Stereotaxic
Reason for recall
Brainlab Knee Navigation System: Femoral and Tibial Cutting Block Adapter Base with specific serial numbers might contain parts made from incorrect material and therefore not be suitable for reprocessing
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0959-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.