Applied Medical Resources Corp: Medical Device Recall in 2026 - (Recall #: Z-1010-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 11, 2025

Date Posted: January 14, 2026

Recall Number: Z-1010-2026

Event ID: 98191

Reason for Recall:

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

Status: Ongoing

Product Quantity: 450 units

Code Information:

UDI: (01)00607915126582; Lot # 1546141

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated