FDA Adverse Event Malfunction Summary report: N

PENCAN®

MDR report key: 25171041 · Received May 14, 2026

Report

Report Number
25171041
Event Type
Malfunction
Date Received
May 14, 2026
Date of Event
May 28, 2024
Report Date
May 1, 2026
Manufacturer
B. BRAUN MEDICAL INC.
Product Code
OFU
Product Problem
Yes
Report Source
User Facility report
Reporter Location
CT
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Description of Event or Problem · 0

THE EVENT BELOW IS SUSPECTED TO BE PART OF A NATIONAL RECALL FROM HUONS, MFG OF ROUGHLY 8% OF BUPIVACAINE INCLUDED IN THE BBRAUN KITS. KIT LOT #S 0061926831, 0061026831, 0061919584. THE PATIENT PRESENTED FOR CERVICAL CERCLAGE AND A SPINAL ANESTHETIC WAS PLANNED AND ADMINISTERED. DESPITE A TECHNICALLY STRAIGHTFORWARD SPINAL AND INJECTION OF 1ML OF HYPERBARIC 0.75% BUPIVACAINE FROM THE SPINAL KIT INTO THE CEREBROSPINAL FLUID, NO DETECTABLE ANESTHETIC LEVEL WAS OBTAINED AND THE PATIENT INSTEAD RECEIVED GENERAL ANESTHESIA FOR THE PROCEDURE. I AM ALSO AWARE OF TWO OTHER SIMILAR EVENTS WITH OTHER ANESTHESIOLOGISTS (DR. [REDACTED] AND DR. [REDACTED]) THAT HAVE OCCURRED IN THE LAST COUPLE OF MONTHS. [REDACTED] CORPORATE SUPPLY CHAIN NOTIFIED VIA EMAIL. [REDACTED] PER DR. [REDACTED], NOT REPORTED AS OCCURRING AT [REDACTED]. [REDACTED] BOTH DRS. [REDACTED] AND [REDACTED] HAVE HAD SPINAL ANESTHETICS WITH HYPERBARIC BUPIVACAINE FROM THE KIT THAT FAILED DESPITE TECHNICALLY STRAIGHT-FORWARD PROCEDURES IN THE LAST COUPLE WEEKS. DR. [REDACTED] TOLD ME ABOUT HERS, AND THEN WHEN DR. [REDACTED] HAD ONE A WEEK LATER, I ASKED HIM TO TAKE A PIC OF THE KIT LOT # SO WE CAN INVESTIGATE SINCE IT SEEMS LIKE A BIG COINCIDENCE. THEY ARE QUESTIONING THE EFFICACY OF THE INCLUDED BUPIVACAINE 0.75% W/ DEXTROSE 8.25%. THIS IS THE BBRAUN PENCAN SPINAL NEEDLE TRAY REF#333851 THAT IS IN USE AT [REDACTED], [REDACTED] AND [REDACTED]. MANUFACTURER RESPONSE FOR MEDICATION, ANESTHETIC, BUPIVACAINE (PER SITE REPORTER). BBRAUN COMPLETED AN INVESTIGATION AND SENT US A LETTER SAYING THEY HAD CONFIRMED WITH THEIR MANUFACTURER (UN-NAMED) THAT THE MEDICATION WAS FINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
139773 PENCAN® SPINAL ANESTHESIA KIT OFU B. BRAUN MEDICAL INC. 333851 0061926831, 0061026831,

Patients

Seq Age Sex Outcome Treatment
1 NA Female Other