FDA Adverse Event Malfunction Summary report: N

PEN NDL 32G 4MM PRO 100 BOX 1200 US

MDR report key: 21416772 · Received February 19, 2025

Report

Report Number
3023359743-2025-00134
Event Type
Malfunction
Date Received
February 19, 2025
Report Date
March 25, 2025
Manufacturer
EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND
Product Code
FMI
UDI-DI
00382903205509
PMA / PMN Number
K212015
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

CORRECTION TO: H6 (COMPONENT CODE, INVESTIGATION FINDINGS, AND INVESTIGATION CONCLUSIONS) INVESTIGATION SUMMARY: SAMPLES WERE RECEIVED AND AN INVESTIGATION WAS PERFORMED. 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. EMBECTA WAS ABLE TO DUPLICATE OR CONFIRM THE INDICATED ISSUE AND BASED ON TREND ANALYSIS NO FURTHER ACTION IS REQUIRED AT THIS TIME. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. BASED ON THE ABOVE, NO ADDITIONAL INVESTIGATION AND CORRECTIVE/PREVENTATIVE ACTION (CAPA) OR SITUATIONAL ANALYSIS (SA) IS REQUIRED.

Description of Event or Problem · 0

CONSUMER REPORTED PATIENT AND NONPATIENT END NEEDLES MISSING FROM 2 NEEDLE HUBS. CONSUMER ALSO REPORTED TEAR DROP LABELS MISSING FROM THE SAME 2 NEEDLE HUBS. SHE STATED THAT THE NEEDLES WITH THE ISSUES WERE AT THE BOTTOM OF THE BOX. LOT #: 4072029, CATALOG #: 320550, DATE OF EVENT: UNKNOWN, SAMPLES: AVAILABLE - SENDING MAIL KIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1039317 PEN NDL 32G 4MM PRO 100 BOX 1200 US NEEDLE, HYPODERMIC, SINGLE LUMEN FMI EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND 320550 4072029 00382903205509

Patients

Seq Age Sex Outcome Treatment
1 NA Female