Integra Cadence Total Ankle System — Class II medical device recall Z-1192-2017
Terminated recall by Integra LifeSciences Corp., reported 2017-02-22, distributed nationwide. Posterior tibial fractures have been reported.
| Recall number | Z-1192-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Integra LifeSciences Corp., Plainsboro, NJ, United States |
| Recall initiated | 2017-01-20 |
| Classified | 2017-02-10 |
| Reported by FDA | 2017-02-22 |
| Terminated | 2017-03-30 |
| Distributed | Nationwide (US) |
| Quantity | 944 units |
| Reason classes | device malfunction |
| Lot numbers | 10207101, 10207102, 10207103, 10207104, 10207105, 10207111, 10207112, 10207113, 10207114, 10207201, 10207202, 10207203, 10207204, 10207205, 10207211, 10207212, 10207213, 10207214, QJ0227, QJ0227-G, QJ0228, QJ0228-G, QJ0231, QJ0231-G, QJ0232, QJ0232-G, QJ0233, QJ0234, QJ0234-G, QJ0235, QJ0235-1, QJ0235-1-G, QJ0236, QJ0236-1, QJ0236-1-1G, QJ0236-1G, QJ0237, QJ0237-1G, QJ0237-G, QJ02371 and 74 more |
Product
Integra Cadence Total Ankle System
Reason for recall
Posterior tibial fractures have been reported.
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-1192-2017. 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.