LITe Decompression Snake Arm — Class II medical device recall Z-0610-2024
Ongoing recall by Stryker Spine, reported 2023-12-27, distributed in MD, MI, NM, TX. Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot
| Recall number | Z-0610-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Spine, Allendale, NJ, United States |
| Recall initiated | 2023-11-01 |
| Classified | 2023-12-21 |
| Reported by FDA | 2023-12-27 |
| Distributed | MD, MI, NM, TX |
| Countries outside the US | CA, FR |
| Quantity | 9 |
| UPC / GTIN / UDI-DI | 07613327263909 |
| Lot numbers | 227764 |
| Model numbers | 48080230 |
Product
LITe Decompression Snake Arm, REF 48080230
Reason for recall
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0610-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.