Recall Z-0313-2022 ยท JDG Prosthesis, Hip, Femoral Component, Cemented, Metal
Howmedica Osteonics Corp.
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028
| Date | Oct 15, 2021 |
| Status | Open, Classified |
| Reason | XXX |
| Root cause | Under Investigation by firm |
| Action | On 10/15/2021, Stryker issued Urgent Medical Device Recall notices to customers. Actions Needed: 1. Please inform users of this Urgent Medical Device Recall and forward this notice to all individuals who need to be made aware. 2. Immediately check all stock areas and/or operating room storage to determine if any devices from the affected product list are at your facility. 3. Quarantine and discontinue use of the recalled devices identified in the affected product list. Return the devices back to Stryker. 4. Hospitals/Branches/Agencies: Complete and sign the enclosed Urgent Medical Device R |
| Distribution | Puerto Rico |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K173499 | Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral Heads Stryker Orthopaedics, Mar 19, 2018 |