FDA Device recall Z-1941-2020
VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628
- FDA Device
- Class II
- terminated
- Published 2020-05-20
On 2020-05-20 the FDA classified a Class II recall of VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628 by Medtronic Sofamor Danek Usa, citing nonconforming product; length of the product measured shorter than the labeled length.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1941-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-03-26 |
| Published | 2020-05-20 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medtronic Sofamor Danek Usa |
| Distribution | US |
Product
VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628
Reason
Nonconforming product; length of the product measured shorter than the labeled length.
Identifiers
| code_info | Product no. 6958838. UDI: 00613994354686. |
|---|
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-1941-2020%22
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