Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Endoscopic Kittner Blunt Dissecting Instrument Recalled by ASPEN SURGICAL Due to The affected products may have been packaged with...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact ASPEN SURGICAL directly.
Affected Products
Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101
Quantity: 1900 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ASPEN SURGICAL
ASPEN SURGICAL has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report