# FDA recall Z-0180-2018

> **Arrow International Inc** · Class II · device recall initiated 2017-06-01.

## Product

ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet  The Pressure Injectable PICC is indicated for short or long term peripheral access to the central venous system for intravenous therapy, blood sampling, infusion, power injection of contrast media and allows for central venous pressure monitoring

## Reason for recall

There is a possibility that the finished good kits may contain 5 Fr peel-away sheaths instead of the required 4 Fr peel-away sheaths.

## Distribution

Nationwide Distribution to AZ, CA, MA, MO, NC, NY, OR & SD

## Key facts

- **Recall number:** Z-0180-2018
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-01
- **Report date:** 2017-12-06
- **Termination date:** 2020-04-13

- **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-0180-2018

## Citation

> AI Analytics. FDA recall Z-0180-2018. Retrieved 2026-06-04 from https://api.ai-analytics.org/recall/Z-0180-2018. Source: US FDA. Licensed CC0.

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