PEN NDL 31GA 5MM 100BX 1200 USA
Report
- Report Number
- 3023359743-2024-00389
- Event Type
- Malfunction
- Date Received
- August 23, 2024
- Date of Event
- November 5, 2024
- Report Date
- August 23, 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 INFORMATION WAS ADDED TO: B4, G6, H2, H3, H11. 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.
CONSUMER REPORTED WHEN INJECTING HER BASLAGAR INSULIN SHE RECEIVED HALF HER DOSE. THE PEN NEEDLE CLOGGED. PROVIDED CONSUMER LILLY PHONE NUMBER. FIRST TIME INJECTING WITH PENS. INFORMED PROPER PLACEMENT OF NON PATIENT END AND TO COMPLETE A FLOW CHECK. DC LOT # 0070045. CATALOG#320119. DATE OF EVENT JULY 28, 2024. SAMPLE STATUS DISCARD.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1313428 | PEN NDL 31GA 5MM 100BX 1200 USA | NEEDLE, HYPODERMIC, SINGLE LUMEN | FMI | EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND | 320119 | 0070045 | 00382903201198 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |