LINK SymphoKnee Patella Sizing Template — Class II medical device recall Z-2445-2024
Ongoing recall by LINK BIO CORP, reported 2024-07-31, distributed nationwide. The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument
| Recall number | Z-2445-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | LINK BIO CORP, Dover, NJ, United States |
| Recall initiated | 2024-06-27 |
| Classified | 2024-07-25 |
| Reported by FDA | 2024-07-31 |
| Distributed | Nationwide (US) |
| Quantity | 8 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04026575310203 |
| Lot numbers | C225066 |
| Model numbers | 881-509/00 |
Product
LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00
Reason for recall
The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.
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-2445-2024. 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.