Recall
FDAHealthSeptember 24, 2025

Aesculap Inc — 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 Compo

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
September 24, 2025

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.

What's affected?

Product
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
Lot code
52974276

Additional details

Model No EK087P; UDI-DI: 04046963620059; Lots 52974276, 52952133, 52954633, 52959357, 52964442, 52968887, 52972214, 52977427, 52981208, 52985519, 52988828, 52992514, 52993617, 52997919, 53002094, 53004347, 53006380, 53007625, 53010869, 53013557

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 155 units.

View original FDA notice →

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