PEN NDL 32G 4MM PRO 100 BOX 1200 US
Report
- Report Number
- 3023359743-2024-00092
- Event Type
- Malfunction
- Date Received
- May 14, 2024
- Date of Event
- April 18, 2024
- Report Date
- August 7, 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 INFORMATION WAS ADDED TO: B4, G6, H2, H3, H11. 3 PEN NEEDLES WERE AFFECTED BY THIS ISSUE. CORRECTION TO: D3 (COUNTRY TYPE AND COUNTRY), 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.
H3 OTHER TEXT : DEVICE IS NOT AVAILABLE.
CONSUMER REPORTED DURING THE INJECTION THE NEEDLE CLOGGED. WENT THROUGH 3 NEEDLES FOR 1 INJECTION LAST NIGHT - NEW TO TAKING INJECTIONS. DC LOT #3130669 CATALOG# 320550 DATE OF EVENT (B)(6) 2024 SAMPLE STATUS DISCARD.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 708763 | PEN NDL 32G 4MM PRO 100 BOX 1200 US | NEEDLE, HYPODERMIC, SINGLE LUMEN | FMI | EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND | 320550 | 3130669 | 00382903205509 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |