# FDA recall Z-1237-2020

> **Arrow International Inc** · Class II · device recall initiated 2019-12-20.

## Product

Arrow FlexTip Plus(R) Epidural Catheterization Kit  ASK-17019-MSC

## Reason for recall

Product lidstock contains the incorrect expiration date for the product

## Distribution

Nationwide  Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA

## Key facts

- **Recall number:** Z-1237-2020
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-20
- **Report date:** 2020-02-26
- **Termination date:** 2021-02-25

- **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-1237-2020

## Citation

> AI Analytics. FDA recall Z-1237-2020. Retrieved 2026-05-23 from https://api.ai-analytics.org/recall/Z-1237-2020. Source: US FDA. Licensed CC0.

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