Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The… — Class II medical device recall Z-1283-2015
Terminated recall by Stryker Howmedica Osteonics Corp., reported 2015-03-25, distributed nationwide. Potential for weld disassociation of the cross pin, which could lead to loose or disassociated trigger mechani
| Recall number | Z-1283-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Howmedica Osteonics Corp., Mahwah, NJ, United States |
| Recall initiated | 2015-02-12 |
| Classified | 2015-03-16 |
| Reported by FDA | 2015-03-25 |
| Terminated | 2016-07-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CH, ES, FR, GB, HK, IE, IN, IT, KR, NL, NZ, PA, SE, ZA |
| Quantity | 2,030 units |
| Model numbers | 6541-1-723 |
Product
Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon Distal Capture Assembly is used when a surgeon elects to use a capture for the distal femoral resection or proximal tibial resection in a Triathlon primary total knee arthroplasty (TKA).
Reason for recall
Potential for weld disassociation of the cross pin, which could lead to loose or disassociated trigger mechanism on the Distal Capture Assembly.
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-1283-2015. 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.