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Recall Observatory FDA recall evidence

Device product

PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13

Z-2579-2021

April 16, 2021

Class II

Product summary

Firm
Aesculap Implant Systems LLC
Event
Event 88327
Status
Terminated
Classification
Class II
Quantity
350 units
Official record key
device-enforcement:Z-2579-2021

Official wording

Reason: 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

Code information: All batch codes

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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