FDA Adverse Event Malfunction Summary report: N

PEN NDL 32G 6MM 3B TW 100CT US

MDR report key: 21446888 · Received February 24, 2025

Report

Report Number
3023359743-2025-00151
Event Type
Malfunction
Date Received
February 24, 2025
Report Date
February 24, 2025
Manufacturer
EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND
Product Code
FMI
UDI-DI
00382903207497
PMA / PMN Number
K213478
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, 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 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.

Description of Event or Problem · 0

CONSUMER LEFT VOICEMAIL REPORTING THAT THE OUTER COVER WILL NOT STAY ON THE NEEDLE WHEN SHE ATTACHES IT TO THE INSULIN PEN. I RETURNED CONSUMER'S CALL AND SHE STATED THAT THE COVER IS LOOSE AND FALLS OFF WHEN SHE ATTACHES IT TO THE PEN. CONSUMER REFUSED REPLACEMENT. SHE SAID SHE GETS THEM FROM THE VA. LOT #: 3073557. CATALOG #: 320749. DATE OF EVENT: UNKNOWN. SAMPLES: DISCARDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
409790 PEN NDL 32G 6MM 3B TW 100CT US Needle, hypodermic, single lumen FMI EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND 320749 3073557 00382903207497

Patients

Seq Age Sex Outcome Treatment
1 NA Prefer Not To Disclose