FDA Adverse Event Malfunction Summary report: N

PEN NDL 32G 4MM 90 CT MAIL ORDER ONLY

MDR report key: 19852181 · Received July 29, 2024

Report

Report Number
3023359743-2024-00329
Event Type
Malfunction
Date Received
July 29, 2024
Report Date
October 16, 2024
Manufacturer
EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND
Product Code
FMI
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

ADDITIONAL INFORMATION WAS ADDED TO: B4, G6, H2, H3, H11. CORRECTION TO: H6 (TYPE OF INVESTIGATION AND INVESTIGATION CONCLUSIONS) INVESTIGATION SUMMARY: NO SAMPLES (INCLUDING PHOTOS) WERE RETURNED THEREFORE THE COMPLAINT COULD NOT BE CONFIRMED AND THE ROOT CAUSE IS UNDETERMINED. 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.

Description of Event or Problem · 0

RECEIVED VOICEMAIL FROM CONSUMER STATING HIS PEN NEEDLES DO NOT WORK. STATED, HE IS THROWING AWAY 30% OF THE PRODUCT DUE TO NEEDLE CLOG. RETURNED CALL. CONSUMER REPORTED, NO INSULIN FLOW WHEN PRIMING HIS PEN NEEDLES. CONSUMER PRIMES 2 UNITS. STATED, HE'S HAD THIS ISSUE OCCUR IN A COUPLE OF BOXES BUT IS ONLY REPORTING ONE LOT NUMBER AND ONE BOX TODAY BECAUSE THE OTHER BOX WAS DISCARDED. LOT: 3241370. CATALOG: 320883. DATE OF EVENT: UNKNOWN. SAMPLES: NO CL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
375050 PEN NDL 32G 4MM 90 CT MAIL ORDER ONLY NEEDLE, HYPODERMIC, SINGLE LUMEN FMI EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND 320883 UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 NA Male