Medical device recalls Moderate risk

Aesculap Inc recalls Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Model/Catalog Number: EK086P Software Version: N/A…

Recall date
September 24, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0311-2026
FDA classification
Class II
Brand / firm
Aesculap Inc
Sold / distributed
Worldwide - US Nationwide distribution in the states of AR, AZ, CA, CT, MD, NE, NM, NY, OR, PA, WA, WI and the country of Canada.

Why it was recalled

It was determined there is the potential of silicone fragments detaching from the yellow sealing component.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Model/Catalog Number: EK086P Software Version: N/A Product Description: SEALING UNIT FOR 10/12MM TROCARS Component: N/A

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