Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | ongoing |
| Recall date | December 11, 2025 |
| Reported | January 14, 2026 |
| Recalling firm | Applied Medical Resources Corp |
| Country / region | United States CA |
Hazard
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
Affected products
- Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
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