# FDA recall Z-0837-2020

> **Arrow International Inc** · Class II · device recall initiated 2019-12-06.

## Product

Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH

## Reason for recall

Potential sterility issue for specific lots of  the Arrow Endurance" Extended Dwell Peripheral Catheter System, Product Code ASK-00820-FLH.

## Distribution

US: FL

## Key facts

- **Recall number:** Z-0837-2020
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-06
- **Report date:** 2020-01-29
- **Termination date:** 2021-11-02

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0837-2020

## Citation

> AI Analytics. FDA recall Z-0837-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0837-2020. Source: US FDA. Licensed CC0.

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