FDAJune 3, 2024device

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

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Completed

Brands named

aspen surgicalaspen

UPCs

00840113214006

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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