PEN NDL 31GA 8MM 100 BX 1200 USA
Report
- Report Number
- 3023359743-2025-00150
- Event Type
- Malfunction
- Date Received
- February 24, 2025
- Date of Event
- January 30, 2025
- Report Date
- February 24, 2025
- Manufacturer
- EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND
- Product Code
- FMI
- UDI-DI
- 00382903201099
- PMA / PMN Number
- K213478
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER
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 FOUND 1 PEN NEEDLE TO CLOG DURING INJECTION. TRIED INJECTING 4 TIMES WITH THIS PEN NEEDLE. INFORMED CALLER OF NON PATIENT END PLACEMENT AND TO COMPLETE A FLOW CHECK WITH ALL INJECTIONS LOT # 4030373 CATALOG# 320109 DATE OF EVENT JANUARY 30 2025 SAMPLE STATUS DISCARD.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 409767 | PEN NDL 31GA 8MM 100 BX 1200 USA | Needle, hypodermic, single lumen | FMI | EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND | 320109 | 4030373 | 00382903201099 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Prefer Not To Disclose |