Aesculap Implant Systems LLC: Medical Device Recall in 2021 - (Recall #: Z-2578-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU

Product Classification:

Class II

Date Initiated: April 16, 2021

Date Posted: October 6, 2021

Recall Number: Z-2578-2021

Event ID: 88327

Reason for Recall:

Malfuncton-Implant did not deploy successfully may necessitate the need for an additional medical intervention for patients which would result in a potential delay in surgery

Status: Terminated

Product Quantity: 80 units

Code Information:

All batch codes

Distribution Pattern:

US Nationwide distribution in the states of FL, MI, NY, TX, WI.

Voluntary or Mandated:

Voluntary: Firm initiated