FDA Adverse Event Malfunction Summary report: N

PEN NDL 31GA 5MM 100BX 1200 USA

MDR report key: 18697051 · Received February 13, 2024

Report

Report Number
9616656-2024-05081
Event Type
Malfunction
Date Received
February 13, 2024
Date of Event
January 15, 2024
Report Date
May 8, 2024
Manufacturer
BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND
Product Code
FMI
UDI-DI
00382903201198
PMA / PMN Number
K213478
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION SUMMARY: NO SAMPLES (INCLUDING PHOTOS) WERE RETURNED THEREFORE THE COMPLAINT COULD NOT BE CONFIRMED AND THE ROOT CAUSE IS UNDETERMINED. THIS IS THE 1ST COMPLAINT FOR THE REPORTED LOT NUMBER. A REVIEW OF THE MANUFACTURING RECORDS WAS PERFORMED, AND NO NON-CONFORMANCES WERE RAISED IN ASSOCIATION WITH THIS TYPE OF EVENT FOR THIS LOT. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. IF SAMPLES ARE RECEIVED IN THE FUTURE THE COMPLAINT WILL BE REOPENED FOR FURTHER INVESTIGATION. BASED ON THE ABOVE, NO ADDITIONAL INVESTIGATION AND NO CORRECTIVE/PREVENTATIVE ACTION (CAPA) OR SITUATIONAL ANALYSIS (SA) IS REQUIRED AT THIS TIME.

Additional Manufacturer Narrative · 0

3 PEN NEEDLES AFFECTED FROM THE SAME BOX. H3 OTHER TEXT : DEVICE NOT AVAILABLE.

Description of Event or Problem · 0

CONSUMER REPORTED FOUND 3 PEN NEEDLES THAT CLOGGED DURING INJECTION LOT # 320119, CATALOG# 3052522, DATE OF EVENT 01/15/2024, SAMPLE STATUS DISCARD (B)(6).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2226062 PEN NDL 31GA 5MM 100BX 1200 USA NEEDLE, HYPODERMIC, SINGLE LUMEN FMI BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND 320119 3052522 00382903201198

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown