FDA Adverse Event Malfunction Summary report: N

BD SYRINGE

MDR report key: 21869548 · Received April 18, 2025

Report

Report Number
2243072-2025-00551
Event Type
Malfunction
Date Received
April 18, 2025
Date of Event
March 7, 2025
Report Date
April 24, 2025
Manufacturer
BECTON DICKINSON
Product Code
FMF
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

D.3. FRANKLIN LAKES HAS BEEN LISTED AS THE MANUFACTURER. E.1. ADDRESS WAS NOT LOCATED AND IL WAS USED. G.1. FRANKLIN LAKES HAS BEEN LISTED AS THE MANUFACTURER. H.3. IF A DEVICE EVALUATION AND/OR DEVICE HISTORY REVIEW IS COMPLETED, A SUPPLEMENTAL REPORT WILL BE FILED.

Additional Manufacturer Narrative · 0

(B)(4) FOLLOW UP AS NO PHYSICAL SAMPLE, PICTURE SAMPLE, OR LOT NUMBER WAS PROVIDED FOR EVALUATION BY OUR QUALITY ENGINEER TEAM, A COMPLETE INVESTIGATION COULD NOT BE PERFORMED. THERE ARE CURRENT QUALITY CONTROLS IN PLACE TO DETECT THIS TYPE OF DEFECT DURING THE PRODUCTION PROCESS. BASED ON THE LIMITED INVESTIGATION RESULTS, A CAUSE FOR THE REPORTED INCIDENT COULD NOT BE DETERMINED. SHOULD YOU AGAIN EXPERIENCE ANY PROBLEMS WITH OUR PRODUCT WE WOULD APPRECIATE THE OPPORTUNITY TO CONDUCT A THOROUGH ANALYSIS. EXAMINATION OF THE PRODUCT INVOLVED MAY PROVIDE CLARIFICATION AS TO THE CAUSE FOR THE REPORTED FAILURE.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE BD SYRINGE HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL: UNKNOWN, BATCH#: UNKNOWN. RCC RECEIVED A COMPLAINT VIA EMAIL. COMPLAINT NUMBER(S): (B)(4). PRODUCT SKU: 26001 - DNOSYR 3ML L/L, 153239- DNQSYRINGE 10ML LL BNS, 153245- DNQSYRINGE 5ML LL BNS. PRODUCT LOT NUMBER: UNKNOWN. COMPLAINT DETAILS: GOOD MORNING, ALL. I HAVE BEEN NOTIFIED AS OF THIS MORNING ON (B)(6) 2025 THAT THREE OF THE PHYSICIANS AT OUR FACILITY HAVE REPORTED SYRINGES SPECIFICALLY FROM OUT PROCEDURE TRAYS DYNJRA1955A HAVE BEEN LEAKING. THERE ARE NO REPORTS OF ANY OTHER OF OUR SYRINGE SUPPLIES HAVING THIS ISSUE, IT JUST SEEMS TO BE THE SYRINGES THAT ARE IN THE TRAYS. IT IS NOT ONE SIZE SYRINGE; IT APPEARS TO BE RANDOMLY ALL OF THEM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1787403 BD SYRINGE PISTON SYRINGE FMF BECTON DICKINSON UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown