Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm Ref: Ctb23

Recall Summary Applied Medical Resources is recalling Kii Low Profile Bladed Dual Packs (5x55mm, REF: CTB23) because the blade obturator may extend beyond its proper length after being assembled into the cannula and seal housing. This is a Class II recall affecting the medical device product.

Recalling firm

Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

Product

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

Reason

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

Classification

Class II

Category

consumer product recall

Country

United States

Agency

FDA-DEVICES

Recall date

2025-12-11

Status

Open, Classified

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2aea336b-60ee-450d-929e-5c9bd43648b4