ASPEN SURGICAL: Medical Device Recall in 2024 - (Recall #: Z-2221-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101

Product Classification:

Class II

Date Initiated: June 3, 2024

Date Posted: July 3, 2024

Recall Number: Z-2221-2024

Event ID: 94778

Reason for Recall:

The affected products may have been packaged with a defect in the sterile barrier seal. As a result, the integrity of the sterile barrier may be compromised.

Status: Ongoing

Product Quantity: 1900 units

Code Information:

UDI-DI: 00840113214006; Lot Numbers: 389571, 389576, 390981, 390982

Distribution Pattern:

US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated