SYRINGE 0.5ML 31GA 8MM 10 BAG 500 WAL
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
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.
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 |