FDA Device recall Z-0786-2022
Wright Medical Technology, Inc
- FDA Device
- Class II
- terminated
- Published 2022-03-23
On 2022-03-23 the FDA classified a Class II recall of Wright Medical Technology, Inc by Wright Medical Technology, citing an incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0786-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-02-15 |
| Published | 2022-03-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Wright Medical Technology |
| Distribution | n/a |
Product
Wright Medical Technology, Inc. ORTHOLOC Non-Locking Screw 2mm x 8mm, REF 5201120008, non-sterile, a component of the ORTHOLOC 2.0/2.4 Plate System.
Reason
An incorrect screw is packaged in the product, which contains a locking screw instead of a non-locking screw.
Identifiers
| code_info | Lot #73967511638696 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0786-2022%22
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