FDA Adverse Event Malfunction Summary report: N

BD 10ML SYRINGE

MDR report key: 21676801 · Received March 24, 2025

Report

Report Number
MW5168011
Event Type
Malfunction
Date Received
March 24, 2025
Date of Event
March 17, 2025
Report Date
March 18, 2025
Manufacturer
BECTON DICKINSON AND COMPANY
Product Code
FMF
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
KS, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Description of Event or Problem · 0

SEVERAL SYRINGES FOUND WITH MISSING OR PARTIAL MARKINGS. BD 50ML SYRINGE #3 LOT:5017162, EXP:12/31/2029, BD 10ML SYRINGE #1 LOT: 5022493, EXP:12/31/2029. BD SMARTSITE BAG ACCESS DEVICE PORT BREAKS OFF WHILE ATTACHING SYRINGE. #2 LOT: 24045736, EXP:04/26/2027 0 DEFECTED PRODUCTS WERE USED FOR PATIENT CARE. ALL DEFECTED ITEMS WERE DISPOSED OF IN THE MOMENT. NO PATIENTS AFFECTED. REFERENCE REPORTS: MW5168009, MW5168010.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2099988 BD 10ML SYRINGE SYRINGE, PISTON FMF BECTON DICKINSON AND COMPANY 5022493

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown BD 50ML SYRINGE| BD SMARTSITE BAG ACCESS DEVICE