LCS Complete Knee Revision System VVC Insert Product Usage: LCS VVC… — Class II medical device recall Z-0703-2017
Terminated recall by DePuy Orthopaedics, Inc., reported 2016-12-14, distributed in TN. DePuy Orthopaedics, Inc. is voluntarily recalling one lot of the LCS Complete Knee Revision System VVC Insert
| Recall number | Z-0703-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Orthopaedics, Inc., Warsaw, IN, United States |
| Recall initiated | 2016-11-08 |
| Classified | 2016-12-03 |
| Reported by FDA | 2016-12-14 |
| Terminated | 2017-06-05 |
| Distributed | TN |
| Quantity | 1 |
| UPC / GTIN / UDI-DI | 10603295024484 |
| Lot numbers | C08294 |
| Expiration dates | 2021-03-31 |
Product
LCS Complete Knee Revision System VVC Insert Product Usage: LCS VVC Insert is used in Knee Revision Surgery
Reason for recall
DePuy Orthopaedics, Inc. is voluntarily recalling one lot of the LCS Complete Knee Revision System VVC Insert Small 22.5mm, due to the insert being manufactured outside of specifications, which prevents the insert from properly seating in the mating tibial tray.
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-0703-2017. 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.