medical Class II Updated 2021-10-06

Aesculap Implant Systems LLC recalls PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-

Recalled Product

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

Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All batch codes
View official government recall

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