# FDA recall Z-0601-2018

> **Arrow International Inc** · Class II · device recall initiated 2017-07-25.

## Product

ARROW PICC powered by ARROW VPS Stylet, Product Codes: CDC-35052-VPS and CDC-35041-VPS.  Peripherally Inserted Central Catheter

## Reason for recall

Finished good kits may contain incorrect components. Kits that should contain a 5 FR 2 lumen catheter may contain a 4 FR single lumen catheter and kits that should contain a 4 FR single lumen catheter may contain a 5 FR 2 lumen catheter. This may cause a delay in treatment while a replacement catheter is obtained.

## Distribution

US nationwide distribution.

## Key facts

- **Recall number:** Z-0601-2018
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-25
- **Report date:** 2018-02-21
- **Termination date:** 2018-08-29

- **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-0601-2018

## Citation

> AI Analytics. FDA recall Z-0601-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0601-2018. Source: US FDA. Licensed CC0.

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