Class II

Medical Device Recall: Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23

Applied Medical Resources Corp · December 11, 2025

Reason for Recall

There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.

Distribution

US: MI, CA, ME, OUS: France Great Britain, Germany

States Affected

CA, ME, MI

Quantity Affected

450 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1010-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.