PEN NDL 32G 4MM PRO 100 BOX 1200 US
Report
- Report Number
- 9616656-2024-05188
- Event Type
- Malfunction
- Date Received
- March 28, 2024
- Report Date
- June 19, 2024
- Manufacturer
- BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, 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
H3 OTHER TEXT : DEVICE NOT AVAILALBE.
ADDITIONAL INFORMATION WAS ADDED TO: B4, G6, H2, H3, H11. 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.
SPOUSE OF CONSUMER REPORTED NEEDLE CLOG DURING INJECTION, STATED THAT THERE IS NO INSULIN FLOW. ALSO STATED THAT THE PEN JAMS SOMETIMES DURING INJECTION. LOT #: 3073545. CATALOG #: 320550. DATE OF EVENT: UNKNOWN. SAMPLES: DISCARDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1153661 | PEN NDL 32G 4MM PRO 100 BOX 1200 US | NEEDLE, HYPODERMIC, SINGLE LUMEN | FMI | BECTON DICKNSON AND CO. - DUN LAOGHAIRE CO, IRELAND | 320550 | 3073545 | 00382903205509 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |