FDA Adverse Event Malfunction Summary report: N

PEN NDL 32G 4MM PRO 100 BOX 1200 CA

MDR report key: 21718442 · Received March 28, 2025

Report

Report Number
3023359743-2025-00245
Event Type
Malfunction
Date Received
March 28, 2025
Report Date
March 28, 2025
Manufacturer
EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND
Product Code
FMI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

THIS MEDWATCH REPORT IS BOTH AN INITIAL AND FINAL SUBMISSION AS THE INVESTIGATION HAS BEEN COMPLETED. INVESTIGATION SUMMARY: NO SAMPLES (INCLUDING PHOTOS) WERE RETURNED THEREFORE THE COMPLAINT COULD NOT BE CONFIRMED AND THE ROOT CAUSE IS UNDETERMINED. THIS IS THE 3RD 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 10 PERCENT OF BOX TO CLOG DURING THE FLOW CHECK. INFORMED CALLER OF THE NON PATIENT END AND PLACEMENT. DC LOT#: 4051705, CATALOG#: 320555, DATE OF EVENT: 03.06.2025 = 2 PEN NEEDLES, DATE OF EVENT: UNKNOWN - UNKNOWN AMOUNT, SAMPLE STATUS: DISCARD ONES WITH ISSUES. CAN SEND UNUSED SAMPLES FROM THIS BOX. DC.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
650354 PEN NDL 32G 4MM PRO 100 BOX 1200 CA Needle, hypodermic, single lumen FMI EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND 320555 4051705

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown