FDA Device recall Z-0566-2020
VALOR SCREW 5.0MM X 45MM LEN, Part Number 4151150045
- FDA Device
- Class II
- terminated
- Published 2019-12-04
On 2019-12-04 the FDA classified a Class II recall of VALOR SCREW 5.0MM X 45MM LEN, Part Number 4151150045 by Wright Medical Technology, citing the firm discovered a lack of adequate documentation confirming sterility on certain products.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0566-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-08 |
| Published | 2019-12-04 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Wright Medical Technology |
| Distribution | n/a |
Product
VALOR SCREW 5.0MM X 45MM LEN, Part Number 4151150045
Reason
The firm discovered a lack of adequate documentation confirming sterility on certain products.
Identifiers
| code_info | Lot Number 1547961 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Other recalls by Wright Medical Technology
- CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System
FDA Device · Class II · 2026-10-07 · Wright Medical Technology - stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
FDA Device · Class II · 2024-04-10 · Wright Medical Technology - Stryker Infinity Alignment Frame Distal Sub-Assembly, Catalog #33600020, non-sterile
FDA Device · Class II · 2023-07-12 · Wright Medical Technology - stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation
FDA Device · Class II · 2023-05-03 · Wright Medical Technology - stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A221RT, bone stabilization and fixation
FDA Device · Class II · 2023-05-03 · Wright Medical Technology
All Wright Medical Technology recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0566-2020%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.