Class IIReported 2026-01-14

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

Recalled by Applied Medical Resources Corp

Reason for Recall

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

Recall Number

Z-1010-2026

Classification

Class II

Status

Ongoing

Category

device

Initiated

2025-12-11

Reported

2026-01-14

Distribution

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

Code Info

UDI: (01)00607915126582; Lot # 1546141

Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.