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Applied Medical Resources Corp recalls Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Recalled January 14, 2026 · FDA recall Z-1010-2026 · Applied Medical Resources
Hazard
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing. · FDA Class II
Units
450 units
Sold at
US: MI, CA, ME, OUS: France Great Britain, Germany
Description
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
Product
Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Manufacturer(s)
Applied Medical Resources Corp
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →