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ASPEN SURGICAL recalls Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101
Recalled July 3, 2024 · FDA recall Z-2221-2024 · ASPEN SURGICAL
Hazard
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. · FDA Class II
Units
1900 units
Sold at
US Nationwide
Description
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.
Product
Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101
Manufacturer(s)
ASPEN SURGICAL
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →