# FDA recall Z-1913-2026

> **ARROW INTERNATIONAL, LLC** · Class II · device recall initiated 2026-03-11.

## Product

FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM  UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409    The Arrow Epidural Catheter kit permits access to the epidural space for administration of  epidural anesthetic. The epidural catheter kit is intended for use up to 72 hours.  The Arrow Combined Spinal Anesthesia and Epidural Catheterization products  permit access to subarachnoid and epidural spaces.  The Arrow Single Shot Epidural product permits access to the epidural space..

## Reason for recall

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

## Distribution

U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.

## Key facts

- **Recall number:** Z-1913-2026
- **Recalling firm:** ARROW INTERNATIONAL, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-11
- **Report date:** 2026-04-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1913-2026

## Citation

> AI Analytics. FDA recall Z-1913-2026. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1913-2026. Source: US FDA. Licensed CC0.

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