FDA Device recall Z-0610-2024
LITe Decompression Snake Arm, REF 48080230
- FDA Device
- Class II
- ongoing
- Published 2023-12-27
On 2023-12-27 the FDA classified a Class II recall of LITe Decompression Snake Arm, REF 48080230 by Stryker Spine, citing product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0610-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-11-01 |
| Published | 2023-12-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Stryker Spine |
| Distribution | MD, MI, NM, TX |
Product
LITe Decompression Snake Arm, REF 48080230
Reason
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
Identifiers
| code_info | UDI-DI (GTIN): 07613327263909, lot # 227764. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0610-2024%22
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