Stryker Blueprint Software — Class II medical device recall Z-1883-2024
Ongoing recall by Tornier S.A.S., reported 2024-05-29, distributed nationwide. The software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anato
| Recall number | Z-1883-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Tornier S.A.S., Montbonnot St Martin, France |
| Recall initiated | 2024-04-16 |
| Classified | 2024-05-22 |
| Reported by FDA | 2024-05-29 |
| Distributed | Nationwide (US) |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 03700434015058, 03700434015065, 03700434023107, 03700434023114 |
| Model numbers | BPUE001 |
Product
Stryker Blueprint Software, Catalog #BPUE001.
Reason for recall
The software bug allows for case planning with anatomic glenoid Perform / Perform Augmented implants and anatomic humeral Tornier Flex implant configurations that are incompatible and do not have regulatory approval.
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-1883-2024. 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.