PEN NDL 32G 4MM 100BX 1200 USA
Report
- Report Number
- 9616656-2024-05011
- Event Type
- Malfunction
- Date Received
- January 8, 2024
- Report Date
- April 2, 2024
- Manufacturer
- BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND
- Product Code
- FMI
- UDI-DI
- 00382903201228
- PMA / PMN Number
- K213478
- 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.
NOT AVAILABLE.
CONSUMER REPORTED NO INSULIN FLOW WHEN TAKING INJECTION. STATED, SHE DOES NOT ALWAYS PRIME THE PEN NEEDLE BEFORE INJECTION. STATED, SHE TAKES 3 INJECTIONS PER DAY AND IS WASTING A LOT OF HER PEN NEEDLES. LOT: 3143587. CATALOG: 320122. DATE OF EVENT: UNKNOWN. SAMPLES: NO CL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 950116 | PEN NDL 32G 4MM 100BX 1200 USA | NEEDLE, HYPODERMIC, SINGLE LUMEN | FMI | BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND | 320122 | 3143587 | 00382903201228 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |