# FDA recall Z-2579-2021

> **Aesculap Implant Systems LLC** · Class II · device recall initiated 2021-04-16.

## 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

## Distribution

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

## Key facts

- **Recall number:** Z-2579-2021
- **Recalling firm:** Aesculap Implant Systems LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-04-16
- **Report date:** 2021-10-06
- **Termination date:** 2023-01-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Center Valley, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2579-2021

## Citation

> AI Analytics. FDA recall Z-2579-2021. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-2579-2021. Source: US FDA. Licensed CC0.

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