OsteoBridge Intramedullary Diaphysis Segment Fixation — Class II medical device recall Z-0436-2021
Terminated recall by Merete Medical GmbH, reported 2020-11-18, distributed in CA, IL, MD, NJ, OH. Product may be mislabeled.
| Recall number | Z-0436-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Merete Medical GmbH, Berlin, Germany |
| Recall initiated | 2020-09-18 |
| Classified | 2020-11-06 |
| Reported by FDA | 2020-11-18 |
| Terminated | 2021-05-13 |
| Distributed | CA, IL, MD, NJ, OH |
| Quantity | 354 units |
| Reason classes | labeling |
| Lot numbers | MS1811571R, MS1811572R, MS1811572R1, MS1811573R, MS1811613R, MS1811614R, MS1811618R, MS1811619R, MS1811620R, MS1811642R, MS1811642R1, MS1811643R, MS1811644R, MS1811645R, MS1811646R, MS1811647R, MS1811660R, MS1811661R, MS1811662R, MS1811663R, MS1811663R1, MS1811664R, MS1811665R, MS1811666R, MS1811667R, MS1811668R, MS1811882R, MS1912441R, MS1912443R, MS1912444R, MS1912446R, MS1913083R, MS1913083R1, MS1913084R, MS1913085R, MS1913086R, MS1913087R, MS1913087R1, MS1913098R, MS1913099R and 20 more |
Product
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (femur)
Reason for recall
Product may be mislabeled.
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-0436-2021. 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.