Stryker, Inc. Recall 93678
Description: Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Stryker, Inc. Recall 93678 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-1084-2024 |
| Event ID | 93678 |
| Event Description | Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm |
| Product Type | Devices |
| Distribution | US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA. |
| Quantity | 11 units |
| Recall Reason | The microcatheter IFU contains an intended use that has not been evaluated by the FDA. |
| Device Classification | 20240221 |
| Device Code Info | UDI: (01)00815742002386/Lot Number(s): 0000228865 0000370674 |
| Center Classification Date | 20240214 |
| Recall Initiation Date | 20231206 |
| Recalling Firm | Stryker, Inc. |
| Initial Notification | Letter |
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