FDA Device recall Z-1507-2016
VariAx Compression Plating System
- FDA Device
- Class II
- terminated
- Published 2016-04-27
On 2016-04-27 the FDA classified a Class II recall of VariAx Compression Plating System by Stryker Howmedica Osteonics, citing stryker received two reports indicating that during screw insertion under a high lateral angle a bone screw went through a oblong hole.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1507-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-10-10 |
| Published | 2016-04-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Howmedica Osteonics |
| Distribution | US |
Product
VariAx Compression Plating System
Reason
Stryker received two reports indicating that during screw insertion under a high lateral angle a bone screw went through a oblong hole.
Identifiers
| code_info | catalog numbers 629503S, 629504S, 629505S, 629506S, 629507S, 629508S, 629509S, 629510S, 629527S, 629537S, 629543S, 629…catalog numbers 629503S, 629504S, 629505S, 629506S, 629507S, 629508S, 629509S, 629510S, 629527S, 629537S, 629543S, 629544S, 629545S, 629546S, 629547S, 629548S, 629559S, 629560S, 629561S, 629562S, 629564S, 629566S, 629568S, 629570S |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1507-2016%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.