FDA Device recall Z-0811-2020
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catal…
- FDA Device
- Class II
- terminated
- Published 2020-01-22
On 2020-01-22 the FDA classified a Class II recall of Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catal… by Howmedica Osteonics, citing may have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0811-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-11-07 |
| Published | 2020-01-22 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Howmedica Osteonics |
| Distribution | CA, FL, GA, IA, MA, MI, NC, OH, WI |
Product
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2041C-3254
Reason
May have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire
Identifiers
| code_info | Lot Number: 53778501 UDIs: (01)04546540035806(17)201108(10)53778501 |
|---|
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-0811-2020%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.