PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13 — Class II medical device recall Z-2579-2021
Terminated recall by Aesculap Implant Systems LLC, reported 2021-10-06, distributed nationwide. Malfuncton-Implant did not deploy successfully may necessitate the need for an additional medical intervention
| Recall number | Z-2579-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aesculap Implant Systems LLC, Center Valley, PA, United States |
| Recall initiated | 2021-04-16 |
| Classified | 2021-09-27 |
| Reported by FDA | 2021-10-06 |
| Terminated | 2023-01-18 |
| Distributed | Nationwide (US) |
| Quantity | 350 units |
| Model numbers | FG-000001-13 |
Product
PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2579-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.