FDA Device recall Z-1673-2015
LCS COMPLETE RPS inserts, various sizes
- FDA Device
- Class II
- terminated
- Published 2015-06-03
On 2015-06-03 the FDA classified a Class II recall of LCS COMPLETE RPS inserts, various sizes by Depuy Orthopaedics, citing the LCS COMPLETE RPS Knee System has higher rates of revision in Australia when the native patella is not resurfaced when compared to other unresurfaced PS implants. If the LCS CO….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1673-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-04 |
| Published | 2015-06-03 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Depuy Orthopaedics |
| Distribution | US |
Product
LCS COMPLETE RPS inserts, various sizes. Knee prosthesis component for orthopedic surgery.
Reason
The LCS COMPLETE RPS Knee System has higher rates of revision in Australia when the native patella is not resurfaced when compared to other unresurfaced PS implants. If the LCS COMPLETE RPS Knee System is implanted and the native patella is not resurfaced, the patient may experience patello-femoral pain, potentially requiring a secondary procedure.
Identifiers
| code_info | All Lots. Catalog numbers: 129416110 129416112 129416115 129416117 129416120 129416122 129416125 129416210 12…All Lots. Catalog numbers: 129416110 129416112 129416115 129416117 129416120 129416122 129416125 129416210 129416212 129416215 129416217 129416220 129416222 129416225 129416310 129416312 129416315 129416317 129416320 129416322 129416325 129416410 129416412 129416415 129416417 129416420 129416422 129416425 129416510 129416512 129416515 129416517 129416520 129416522 129416525 129416610 129416612 129416615 129416617 129416620 129416622 129416625 129416710 129416712 129416715 129416717 129416720 129416722 129416725 129417110 129417112 129417115 129417117 129417120 129417122 129417125 129417210 129417212 129417215 129417217 129417220 129417222 129417225 129417310 129417312 129417315 129417317 129417320 129417322 129417325 129417410 129417412 129417415 129417417 129417420 129417422 129417425 129417510 129417512 129417515 129417517 129417520 129417522 129417525 129417610 129417612 129417615 129417617 129 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1673-2015%22
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