FDA Adverse Event Malfunction Summary report: N

PEN NDL 31GA 5MM 100BX 1200 USA

MDR report key: 19533263 · Received June 13, 2024

Report

Report Number
3023359743-2024-00200
Event Type
Malfunction
Date Received
June 13, 2024
Report Date
August 29, 2024
Manufacturer
EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND
Product Code
FMI
UDI-DI
00382903201198
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

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. 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 REPORTED FINDING THE NEEDLES TO CLOG DURING INJECTION. DOES NOT ALWAYS COMPLETE A PROPER FLOW CHECK. INFORMED CALLER OF PROPER PLACEMENT OF NON PATIENT END. LOT # 2172143. CATALOG# 320119. DATE OF EVENT UNKNOWN . SAMPLE STATUS DISCARD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
766803 PEN NDL 31GA 5MM 100BX 1200 USA NEEDLE, HYPODERMIC, SINGLE LUMEN FMI EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND 320119 2172143 00382903201198

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown