FDA Adverse Event Malfunction Summary report: N

PEN NDL 32G 4MM 100BX 1200 USA

MDR report key: 21343901 · Received February 10, 2025

Report

Report Number
3023359743-2025-00096
Event Type
Malfunction
Date Received
February 10, 2025
Report Date
February 10, 2025
Manufacturer
EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND
Product Code
FMI
UDI-DI
00382903201228
PMA / PMN Number
K213478
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER

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 2ND COMPLAINT FOR THE REPORTED LOT NUMBER. A REVIEW OF THE MANUFACTURING RECORDS WAS PERFORMED, AND NO NON-CONFORMANCE'S 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.

Description of Event or Problem · 0

CONSUMER REPORTED FINDING NEEDLES TO CLOG DURING THE FLOW CHECK. INFORMED OF PROPER NON-PATIENT END PLACEMENT. DC LOT#: 4142006, CATALOG#: 320122 & UNKNOWN, DATE OF EVENT: UNKNOWN, SAMPLE STATUS: DISCARD, TMAIK: ON (B)(6) 2025, UPDATE: 00022746, CATALOG#: 320122, LOT#: 4142006 - 1 BOX, LOT#: UNKNOWN - ON 1 PRIOR BOX - SAME CATALOG NUMBER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1515077 PEN NDL 32G 4MM 100BX 1200 USA Needle, hypodermic, single lumen FMI EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND 320122 4142006 00382903201228

Patients

Seq Age Sex Outcome Treatment
1 NA Female