FDA Device recall Z-0546-2020
Intersomatic JULIET Ti OL cage
- FDA Device
- Class III
- terminated
- Published 2019-12-04
On 2019-12-04 the FDA classified a Class III recall of Intersomatic JULIET Ti OL cage by Spineart, citing inner blister pack label is incorrect and does not match the correct external box label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0546-2020 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2019-02-05 |
| Published | 2019-12-04 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Spineart |
| Distribution | CA |
Product
Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures
Reason
Inner blister pack label is incorrect and does not match the correct external box label.
Identifiers
| code_info | Model Number: JUT-OX 28 09-S Lot Number: 4-2899 UDI: (01) 0 7640178 97398 5 (11) 181102 (17) 261101 (10) 4-2899 |
|---|
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-0546-2020%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.