Home / Recalls / Medical Devices
Aesculap Implant Systems LLC recalls PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13
Recalled October 6, 2021 · FDA recall Z-2579-2021 · Aesculap Implant Systems
Hazard
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 · FDA Class II
Units
350 units
Sold at
US Nationwide distribution in the states of FL, MI, NY, TX, WI.
Description
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
Product
PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →