FDA Device recall Z-1156-2020
Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010
- FDA Device
- Class II
- terminated
- Published 2020-02-19
On 2020-02-19 the FDA classified a Class II recall of Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010 by Medicrea International, citing inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserter.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1156-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-10-02 |
| Published | 2020-02-19 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medicrea International |
| Distribution | OH, VA |
Product
Medicrea TLIF-B Holder, short intended for Intervertebral body fusion device Catalog: Number A24200010
Reason
Inner draw rod, which threads into the cage may potentially be separated from the proximal knob of the inserter
Identifiers
| code_info | Lot Numbers l9B0570; 19B0572 |
|---|
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-1156-2020%22
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