Aesculap Inc: Medical Device Recall in 2025 - (Recall #: Z-0312-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 24, 2025

Date Posted: November 5, 2025

Recall Number: Z-0312-2026

Event ID: 97649

Reason for Recall:

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

Status: Ongoing

Product Quantity: 155 units

Code Information:

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

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated