Class II

Medical Device Recall: 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

Aesculap Inc · September 24, 2025

Reason for Recall

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

Distribution

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.

States Affected

NATIONWIDE

Quantity Affected

155 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0312-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.