FDA Device recall Z-0496-2019
Vanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108
- FDA Device
- Class II
- terminated
- Published 2018-11-28
On 2018-11-28 the FDA classified a Class II recall of Vanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108 by Zimmer Biomet, citing label on the outer carton or the patient labels does not match label on the inner sterile packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0496-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-10-22 |
| Published | 2018-11-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | AR, MN, MO, NJ, NY, OH, VA |
Product
Vanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108
Reason
Label on the outer carton or the patient labels does not match label on the inner sterile packaging
Identifiers
| code_info | Lot Number: J6265594 UDI: (01)00880304270893(17)280411(10)J6255863 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0496-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.