ARROW INTERNATIONAL, LLC recalls FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code:

Recalled April 29, 2026 · FDA recall Z-1913-2026 · ARROW INTERNATIONAL

Hazard

Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured · FDA Class II

Units

190

Sold at

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

Description

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

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..

Manufacturer(s)

ARROW INTERNATIONAL, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →