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 |