Stryker Spine Recall 88217
Description: Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962
Stryker Spine Recall 88217 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-2100-2021 |
| Event ID | 88217 |
| Event Description | Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962 |
| Product Type | Devices |
| Distribution | US Nationwide Distribution |
| Quantity | 559 total |
| Recall Reason | The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution. |
| Device Classification | 20210728 |
| Device Code Info | lot A1908003 |
| Center Classification Date | 20210720 |
| Recall Initiation Date | 20210518 |
| Recalling Firm | Stryker Spine |
| Initial Notification | Letter |
| Similar To |