FDA Adverse Event Malfunction Summary report: N

PEN NDL 32G 4MM 100BX 1200 USA

MDR report key: 18466110 · Received January 8, 2024

Report

Report Number
9616656-2024-05011
Event Type
Malfunction
Date Received
January 8, 2024
Report Date
April 2, 2024
Manufacturer
BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND
Product Code
FMI
UDI-DI
00382903201228
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

NOT AVAILABLE.

Description of Event or Problem · 0

CONSUMER REPORTED NO INSULIN FLOW WHEN TAKING INJECTION. STATED, SHE DOES NOT ALWAYS PRIME THE PEN NEEDLE BEFORE INJECTION. STATED, SHE TAKES 3 INJECTIONS PER DAY AND IS WASTING A LOT OF HER PEN NEEDLES. LOT: 3143587. CATALOG: 320122. DATE OF EVENT: UNKNOWN. SAMPLES: NO CL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
950116 PEN NDL 32G 4MM 100BX 1200 USA NEEDLE, HYPODERMIC, SINGLE LUMEN FMI BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND 320122 3143587 00382903201228

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown