Stryker Instruments Div. of Stryker Corporation Recall: Stryker 1.5mm Wire Pass Drill Ster
Stryker Instruments Div. of Stryker Corporation Recall: Stryker 1.5mm Wire Pass Drill Ster is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Stryker Instruments Div. of Stryker Corporation; Product: Stryker 1.5mm Wire Pass Drill Sterile Product Usage: The devices are intended to be used
| Recalling firm | Stryker Instruments Div. of Stryker Corporation |
|---|---|
| Product | Stryker 1.5mm Wire Pass Drill Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical applications including maxillofacial, craniofacial surgeries. The main procedures/conditions in which these products are expected to be used are Mastoidectomy/Cochlear implant, Craniotomy, Vertebral Fusion and Fixation and Craniosynostosis. |
| Reason for recall | There may be missing notches, partial notches or no notches at all in some Cutting Accessories that are used with the Elite" Attachments. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide Distribution - US (nationwide) |
| Recall initiated | 20140522 |
| Recall number | Z-1773-2014 |
| Category | device |
| State | MI |
| Country | United States |
$29/mo
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