FDA Device recall Z-1477-2024
stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
- FDA Device
- Class II
- ongoing
- Published 2024-04-10
On 2024-04-10 the FDA classified a Class II recall of stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty by Wright Medical Technology, citing stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an int….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1477-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-06 |
| Published | 2024-04-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Wright Medical Technology |
| Distribution | NE, TX |
Product
stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
Reason
Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the finished instrument assembly. The missing screw is used to lockout the Medial/Lateral adjustment on the INFINITY Resection Adjustment Guide.
Identifiers
| code_info | UDI/DI 00889797004008, Lot Numbers: 2656950, 2762126, 2796094 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1477-2024%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.