Aesculap Inc recalls Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N/A…

Recall date

September 24, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0312-2026

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: REDUCING CONVERTER 10/12MM TO 5MM Model/Catalog Number: EK087P Software Version: N/A Product Description: REDUCING CONVERTER 10/12MM TO 5MM Component: N/A