RecallRadar

FDA Device recall Z-1913-2026

FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(1…

On 2026-04-29 the FDA classified a Class II recall of FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(1… by Arrow International, citing due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1913-2026
ClassificationClass II
Statusongoing
Initiated2026-03-11
Published2026-04-29
Last updated2026-09-13 11:58 UTC
CompanyArrow International
DistributionUS

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

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

Identifiers

code_infoProduct code:ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 Batch Number: 33F25K0409

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1913-2026%22

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