FDA Adverse Event Injury Summary report: N

ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK TRAY - FB-19609-K

MDR report key: 24834675 · Received April 9, 2026

Report

Report Number
MW5186615
Event Type
Injury
Date Received
April 9, 2026
Report Date
April 7, 2026
Manufacturer
TELEFLEX MEDICAL LLC
Product Code
CAZ
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN
Health Professional
*

Narratives

Description of Event or Problem · 0

TWO PATIENTS HAVE DEVELOPED AN INFECTION REQUIRING AN I&D AFTER GOING HOME WITH A PERIPHERAL NERVE BLOCK AND AN ONQ PUMP POST ORTHOPEDIC PROCEDURES. THE LOT NUMBERS OF THE PRODUCT WERE THE ONLY SIMILARITY IDENTIFIED THUS FAR. PT CODE: 1930. DEVICE CODES: 2303, 1631. REF: MW5186614.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
539097 ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK TRAY - FB-19609-K ANESTHESIA CONDUCTION KIT CAZ TELEFLEX MEDICAL LLC 33F25L0351

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Hospitalization| O