FDA Adverse Event Malfunction Summary report: N

BARREL 1CC S/T W/SIL NO BD LOGO/TB BNS

MDR report key: 12522435 · Received September 23, 2021

Report

Report Number
1213809-2021-00654
Event Type
Malfunction
Date Received
September 23, 2021
Date of Event
March 22, 2021
Report Date
September 24, 2021
Manufacturer
BECTON DICKINSON MEDICAL SYSTEMS
Product Code
FMF
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MX
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

THE FOLLOWING FIELDS WERE UPDATED DUE TO ADDITIONAL INFORMATION: D.4. MEDICAL DEVICE LOT #: 9098803. D.4. MEDICAL DEVICE EXPIRATION DATE: UNKNOWN . H.4. DEVICE MANUFACTURE DATE: 8/4/2019. D.4. MEDICAL DEVICE LOT #: 0100479. D.4. MEDICAL DEVICE EXPIRATION DATE: UNKNOWN. H.4. DEVICE MANUFACTURE DATE: 4/9/2020. H.6. INVESTIGATION: SINCE NO SAMPLES DISPLAYING THE REPORTED CONDITION WERE RECEIVED THE REPORTED DEFECT COULD NOT BE CONFIRMED. A DEVICE HISTORY RECORD REVIEW WAS COMPLETED FOR PROVIDED LOT NUMBER 9098803. A REVIEW SHOWED NO REJECTED INSPECTIONS OR QUALITY ISSUES DURING THE PRODUCTION THAT COULD HAVE CONTRIBUTED TO THE REPORTED DEFECT. A DEVICE HISTORY RECORD REVIEW WAS COMPLETED FOR PROVIDED LOT NUMBER 0100479. A REVIEW SHOWED INSUFFICIENT SILICONE ISSUE WAS REPORTED DURING THE PRODUCTION. PRODUCT WAS REQUALIFIED PER APPLICABLE ACCEPTABLE QUALITY LIMIT BEFORE PRODUCTION RESUMED. H3 OTHER TEXT : SEE H.10.

Description of Event or Problem · 0

IT WAS REPORTED WHEN USING THE BARREL 1CC S/T W/SIL NO BD LOGO/TB BNS THERE WAS LEAKAGE. THIS EVENT OCCURRED 603 TIMES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: "THE SYRINGE IS NOT SELF-FILLING. SYRINGE LEAKING BLOOD POST DRAW.".

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

IT WAS REPORTED WHEN USING THE BARREL 1CC S/T W/SIL NO BD LOGO/TB BNS THERE WAS LEAKAGE. THIS EVENT OCCURRED 603 TIMES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: "THE SYRINGE IS NOT SELF-FILLING. SYRINGE LEAKING BLOOD POST DRAW."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1419673 BARREL 1CC S/T W/SIL NO BD LOGO/TB BNS PISTON SYRINGE FMF BECTON DICKINSON MEDICAL SYSTEMS SEE H.10

Patients

Seq Age Sex Outcome Treatment
1