FDA Adverse Event Malfunction Summary report: N

SYR 10ML PUMP COMPATIBLE SALINE 10ML FIL

MDR report key: 22523993 · Received July 16, 2025

Report

Report Number
1911916-2025-00525
Event Type
Malfunction
Date Received
July 16, 2025
Date of Event
July 9, 2025
Report Date
July 31, 2025
Manufacturer
BECTON DICKINSON
Product Code
FOZ
UDI-DI
00382903065479
PMA / PMN Number
K003553
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ID, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

H11: A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Additional Manufacturer Narrative · 0

(B)(4) FOLLOW UP. A DEVICE HISTORY RECORD REVIEW WAS COMPLETED BY OUR QUALITY ENGINEER TEAM FOR PROVIDED MATERIAL NUMBER 306547 AND LOT NUMBER 5091770. THE REVIEW DID NOT REVEAL ANY DETECTED ABNORMALITIES DURING THE PRODUCTION PROCESS THAT COULD HAVE CONTRIBUTED TO THE REPORTED ISSUE, AND ALL QUALITY TESTS WERE FOUND TO BE WITHIN SPECIFICATION. AS A SAMPLE WAS UNAVAILABLE FOR RETURN, A THOROUGH SAMPLE INVESTIGATION COULD NOT BE COMPLETED. BASED ON THE INVESTIGATION RESULTS, AN EXACT CAUSE FOR THIS INCIDENT COULD NOT BE IDENTIFIED. SHOULD YOU AGAIN EXPERIENCE ANY PROBLEMS WITH OUR PRODUCT WE WOULD APPRECIATE THE OPPORTUNITY TO CONDUCT A THOROUGH ANALYSIS. THERE ARE QUALITY CONTROLS CURRENTLY IN PLACE TO DETECT SIMILAR ISSUES DURING THE PRODUCTION PROCESS. FURTHER ACTION HAS NOT BEEN DETERMINED NECESSARY AT THIS TIME.

Description of Event or Problem · 0

DESCRIPTION: 3 MISSING THE SALINE. NO PT HARM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
539248 SYR 10ML PUMP COMPATIBLE SALINE 10ML FIL CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS FOZ BECTON DICKINSON 5091770 00382903065479

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown