Stryker XIA 3 Iliac Screwdriver — Class II medical device recall Z-0893-2013
Terminated recall by Stryker Spine, reported 2013-03-06, distributed nationwide. Surgeons have experienced unthreading of the screwdrivers outer shafts during use.
| Recall number | Z-0893-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Spine, Allendale, NJ, United States |
| Recall initiated | 2012-12-27 |
| Classified | 2013-02-28 |
| Reported by FDA | 2013-03-06 |
| Terminated | 2015-09-30 |
| Distributed | Nationwide (US) |
| Quantity | 46 units |
| Lot numbers | 10E852, 10G637, 10G638 |
| Model numbers | 48231326 |
Product
Stryker XIA 3 Iliac Screwdriver, 3-PCS. The XIA 3 Iliac Screwdriver is used to drive XIA 3 closed head Monoaxial and closed head Polyaxial screws into the Ilium. Orthopedic manual surgical instrument.
Reason for recall
Surgeons have experienced unthreading of the screwdrivers outer shafts during use.
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-0893-2013. 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.