# FDA recall Z-2698-2017

> **Arrow International Inc** · Class II · device recall initiated 2017-06-12.

## Product

Arrow EVOLUTION Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombogenic Technology

## Reason for recall

Arrow is recalling additional lots that were identified as part of an active recall. Arrow is recalling the affected product due to the possibility that the catheter peel-away component hub tabs may prematurely detach when the practitioner begins to peel apart the sheath body from the catheter.

## Distribution

Distributed to SC, AL, NJ, IN, MA, GA, CA, PA, AZ, VA , WA and Bangkok

## Key facts

- **Recall number:** Z-2698-2017
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-12
- **Report date:** 2017-07-19
- **Termination date:** 2018-09-06

- **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-2698-2017

## Citation

> AI Analytics. FDA recall Z-2698-2017. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2698-2017. Source: US FDA. Licensed CC0.

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