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.

Applied Medical Resources Corp Medical Device Recall: Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23 | SafeCheck