BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM
Report
- Report Number
- 3014704491-2022-00381
- Event Type
- Malfunction
- Date Received
- August 29, 2022
- Date of Event
- July 9, 2022
- Report Date
- August 26, 2022
- Manufacturer
- BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU
- Product Code
- FOZ
- PMA / PMN Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
IN RESPONSE TO THE EVENT REPORTED BY YOUR FACILITY A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 1230655. OUR RECORDS SHOW THAT THIS IS THE ONLY INSTANCE OF THIS ISSUE OCCURRING IN THIS PRODUCTION BATCH. ACCORDING TO THE SAMPLING PLAN APPLIED FOR PRODUCT PERFORMANCE, THIS LOT WAS ACCEPTED AND RELEASED WITHOUT DEFECTS BEING NOTED DURING THE FINAL ASSEMBLY OR VISUAL INSPECTIONS. A SAMPLE COULD NOT BE OBTAINED FOR EVALUATION AND TESTING; IN LIEU OF THE AFFECTED DEVICE, FUNCTIONAL TESTING WAS PERFORMED ON RETENTION SAMPLES FOR THIS LOT, THE RESULTS OF THESE SHOW THAT THE TESTED UNITS PERFORMED WITHIN PRODUCT SPECIFICATIONS. UNFORTUNATELY WITHOUT THE ABILITY TO INVESTIGATE THE AFFECTED UNIT OUR QUALITY ENGINEERS WERE UNABLE TO DETERMINE THE ROOT CAUSE FOR THIS COMPLAINT.
IT WAS REPORTED THAT THE BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM EXPERIENCED THE NEEDLE DETACHED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: ON (B)(6) 2022, PREGNANT WOMAN GAVE BIRTH IN THE HOSPITAL TO INTRAVENOUS INFUSION WITH A CLOSED VEIN INDWELLING NEEDLE. BEFORE THE USE, NURSE FOUND THAT THE NEEDLE CAME OUT, AND THE NEEDLE WAS RE-PUNCTURED AFTER REPLACEMENT. (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 148416 | BD INTIMA-II Y 24GAX0.75IN PRN/EC SLM | INTRAVASCULAR CATHETER | FOZ | BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU | 1230655 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown |