FDA Device recall Z-0937-2019
Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764
- FDA Device
- Class II
- terminated
- Published 2019-03-06
On 2019-03-06 the FDA classified a Class II recall of Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764 by Zimmer Biomet, citing vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0937-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-12-21 |
| Published | 2019-03-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Zimmer Biomet |
| Distribution | MN, VA |
Product
Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764
Reason
Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.
Identifiers
| code_info | Lot Number: 399960 UDI Number: (01)00880304431317(17)230302(10)399960 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0937-2019%22
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