FDA Adverse Event Malfunction Summary report: N

PEN NDL 32G 4MM PRO 100 BOX 1200 US

MDR report key: 19558478 · Received June 18, 2024

Report

Report Number
3023359743-2024-00220
Event Type
Malfunction
Date Received
June 18, 2024
Report Date
September 5, 2024
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
US
Reporter Occupation
OTHER
Health Professional
N

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 REPORTED NEEDLE CLOG DURING INJECTION. SHE STATED THAT SHE WAS NOT ABLE TO DEPRESS THE PEN. CONSUMER DOES NOT PRIME. CONSUMER DOES NOT RE-USE. CONSUMER REMOVED THE NEEDLE FROM THE PEN AND PLACED A NEW NEEDLE ON WHILE WE WERE ON THE PHONE AND THE NEW NEEDLE WORKED. WHILE EXAMINING THE NEEDLE CONSUMER NOTICED THAT THE NON PATIENT END WAS BENT. LOT #: 3122192. CATALOG #: 320550. DATE OF EVENT: UNKNOWN. SAMPLES: AVAILABLE - SENDING MAIL KIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2316487 PEN NDL 32G 4MM PRO 100 BOX 1200 US NEEDLE, HYPODERMIC, SINGLE LUMEN FMI EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND 320550 3122192 00382903205509

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown