FDA Device recall Z-0940-2018
Accolade and Restoration hip product
- FDA Device
- Class II
- terminated
- Published 2018-03-21
On 2018-03-21 the FDA classified a Class II recall of Accolade and Restoration hip product by Howmedica Osteonics, citing inner and outer sterile barriers not fully sealed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0940-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-21 |
| Published | 2018-03-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Howmedica Osteonics |
| Distribution | AR, DE, FL, IL, IN, MI, NJ, OH, TN, TX |
Product
Accolade and Restoration hip product; Catalog Number: 6720-0837 and 6721-0737
Reason
Inner and outer sterile barriers not fully sealed.
Identifiers
| code_info | Lot: 56211103, 56211401, 56211704, 57284004 |
|---|
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-0940-2018%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.