FDA Device recall Z-1127-2013
The Oxford Partial Knee
- FDA Device
- Class II
- terminated
- Published 2013-04-24
On 2013-04-24 the FDA classified a Class II recall of The Oxford Partial Knee by Synvasive Technology, citing biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1127-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-03-14 |
| Published | 2013-04-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Synvasive Technology |
| Distribution | US |
Product
The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use with Stryker System 5, System 4, System 2000 and EDH. Product Usage: For use with Stryker System 5, System 4, System 2000 and EDH. A set of three surgical saw blades is used to resect damaged cartilage and/or bone in an orthopedic reconstructive procedure such as a partial knee replacement. The set contains both oscillating blades for tissue resection along a small arc in a left/right or up/down direction, and reciprocating blades for resection back and forth in a single plane.
Reason
Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade.
Identifiers
| code_info | Biomet Product code: 506076, Lot 829182. Synvasive Part Number: 11-3629. |
|---|
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-1127-2013%22
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