Home/Recalls/FDA-Z-1913-2026
FDA DevicesClass II

FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHET...

Published: April 29, 2026Recall ID: Z-1913-2026Category: devicesCountry: US

Reason for Recall / Hazard

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

Product Description & Identification

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..

Affected Products

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..

Additional Source Details

FieldValue
CityMorrisville
StateNC
Event id98618
Address 13015 Carrington Mill Blvd
Address 2N/A
Code infoProduct code:ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 Batch Number: 33F25K0409
Postal code27560-5437
Report date20260429
Product typeDevices
Product quantity190
Reason for recallDue to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260311
Initial firm notificationLetter
Center classification date20260422

Overview

  • Recalling FirmARROW INTERNATIONAL, LLC
  • StatusOngoing
  • Risk LevelClass II
  • DistributionU.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.
Official Agency Alert