# FDA recall Z-0654-2018

> **Arrow International Inc** · Class II · device recall initiated 2017-10-17.

## Product

Arrow Multi Lumen CVC Kit (Central venous catheter); Product Code: CDC-15703-1A; Exp. Dates Feb 2018 - Nov 2018

## Reason for recall

These finished good kits may contain the incorrect Springwire Guide (SWG).

## Distribution

Distribution US Nationwide

## Key facts

- **Recall number:** Z-0654-2018
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-10-17
- **Report date:** 2018-02-28
- **Termination date:** 2020-04-14

- **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-0654-2018

## Citation

> AI Analytics. FDA recall Z-0654-2018. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/Z-0654-2018. Source: US FDA. Licensed CC0.

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