Recall database

Catheter, Conduction, Anesthetic recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–2 of 2 recalls

Class IOngoingZ-2371-2026

ARROW INTERNATIONAL, LLC recalls Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if ster…

Anesthetic Conduction Catheter
Nonconforming Material/Component

ARROW INTERNATIONAL, L…NCJun 24, 2026

Class IIOngoingZ-1913-2026

ARROW INTERNATIONAL, LLC recalls FLEXTIP PLUS EPIDURAL CATHETER

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

Anesthetic Conduction Catheter
Process control

ARROW INTERNATIONAL, L…NCApr 29, 2026