FDA Adverse Event Malfunction Summary report: N

SYRINGE 0.5ML 31GA 8MM 10 BAG 500 WAL

MDR report key: 19754603 · Received July 16, 2024

Report

Report Number
3024508819-2024-00180
Event Type
Malfunction
Date Received
July 16, 2024
Report Date
October 8, 2024
Manufacturer
EMBECTA MEDICAL I LLC - HOLDREGE, NE
Product Code
FMF
UDI-DI
00681131311762
PMA / PMN Number
K190054
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 THAT THE NEEDLES BEND AND BREAK OFF DURING INJECTION. CONSUMER ALSO REPORTED THAT ONE OF THE SYRINGE NEEDLES BROKE OFF IN THE INJECTION SITE. SHE WAS ABLE TO REMOVE THE NEEDLE WITH A TWEEZER WITHOUT INJURY OR DISCOMFORT. THERE WAS NO MEDICAL ATTENTION. CONSUMER DOES NOT RE-USE. LOT #: 2080931; CATALOG #: 328509; DATE OF EVENT: UNKNOWN; SAMPLES: DISCARDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2508366 SYRINGE 0.5ML 31GA 8MM 10 BAG 500 WAL SYRINGE, PISTON FMF EMBECTA MEDICAL I LLC - HOLDREGE, NE 328509 2080931 00681131311762

Patients

Seq Age Sex Outcome Treatment
1 NA Female