FDA Adverse Event Malfunction Summary report: N

BD VACUTAINER® BORIC ACID SODIUM BORATE/FORMATE C&S URINE TUBE

MDR report key: 21406075 · Received February 18, 2025

Report

Report Number
1917413-2025-00134
Event Type
Malfunction
Date Received
February 18, 2025
Date of Event
December 26, 2024
Report Date
March 14, 2025
Manufacturer
BECTON, DICKINSON & CO. (BROKEN BOW)
Product Code
JSM
UDI-DI
50382903649582
PMA / PMN Number
K024240
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

D4. MEDICAL DEVICE EXPIRATION DATE: UNKNOWN. H4. DEVICE MANUFACTURE DATE: UNKNOWN. A DEVICE EVALUATION AND/OR DEVICE HISTORY REVIEW IS ANTICIPATED BUT IS NOT COMPLETE. UPON COMPLETION, A SUPPLEMENTAL REPORT WILL BE FILED.

Additional Manufacturer Narrative · 0

INVESTIGATION SUMMARY: BD HAD NOT RECEIVED ANY SAMPLES FOR INVESTIGATION. THE DEVICE HISTORY RECORDS COULD NOT BE REVIEWED AS THE LOT NUMBER IS UNKNOWN. THIS COMPLAINT HAS NOT BEEN CONFIRMED FOR THE INDICATED FAILURE MODE: STOPPER POP OFF. NO DEFINITIVE ROOT CAUSE COULD BE ESTABLISHED FOR THE REPORTED DEFECT. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. INFORMATION WILL BE CAPTURED ON TREND REPORTS AND MONITORED. OUR BUSINESS TEAM REGULARLY REVIEWS THE COLLECTED DATA FOR THE IDENTIFICATION OF EMERGING TRENDS.

Description of Event or Problem · 0

IT WAS REPORTED THAT WHILE USING BD VACUTAINER® BORIC ACID SODIUM BORATE/FORMATE C&S URINE TUBE, AN UNSPECIFIED NUMBER OF TUBES ARE NOT RESEATING ON THEIR AUTOMATED INSTRUMENT (COPAN WASP); CAPS ARE LOOSE AND CAUSING SPILLS AND SPLASHES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.

Description of Event or Problem · 0

IT WAS REPORTED THAT WHILE USING BD VACUTAINER® BORIC ACID SODIUM BORATE/FORMATE C&S URINE TUBE, AN UNSPECIFIED NUMBER OF TUBES ARE NOT RESEATING ON THEIR AUTOMATED INSTRUMENT (COPAN WASP); CAPS ARE LOOSE AND CAUSING SPILLS AND SPLASHES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2539806 BD VACUTAINER® BORIC ACID SODIUM BORATE/FORMATE C&S URINE TUBE CULTURE MEDIA, NON-PROPAGATING TRANSPORT JSM BECTON, DICKINSON & CO. (BROKEN BOW) UNKNOWN 50382903649582

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown