# FDA recall Z-0844-2020

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

## Product

Arrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018" (0.46 mm) dia. Spring-Wire Guide  Product Code: ASK-04020-PMC     The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels.

## Reason for recall

The lidstock label incorrectly displays a  MR (Magnetic   Resonance ) Conditional  symbol (instead of a  MR Unsafe symbol) in reference to a component of the kit

## Distribution

US distribution to SC

## Key facts

- **Recall number:** Z-0844-2020
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-12-12
- **Report date:** 2020-01-29

- **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-0844-2020

## Citation

> AI Analytics. FDA recall Z-0844-2020. Retrieved 2026-06-01 from https://api.ai-analytics.org/recall/Z-0844-2020. Source: US FDA. Licensed CC0.

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