Class II

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

ASPEN SURGICAL · June 3, 2024

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.

Distribution

US Nationwide

States Affected

NATIONWIDE

Quantity Affected

1900 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2221-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.