FDADecember 11, 2025device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

applied medical resourcesappliedapplied medical

UPCs

00607915126582

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →