BD VACUTAINER® PRECISIONGLIDE¿ MULTIPLE SAMPLE NEEDLE
Report
- Report Number
- 9617032-2024-01489
- Event Type
- Malfunction
- Date Received
- September 19, 2024
- Date of Event
- August 21, 2024
- Report Date
- August 23, 2024
- Manufacturer
- BECTON, DICKINSON AND COMPANY (BD)
- Product Code
- FMI
- UDI-DI
- 30382903602101
- PMA / PMN Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NZ
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
INVESTIGATION SUMMARY: "MATERIAL #: 360210. LOT/BATCH #: 4003277. BD RECEIVED 30 SAMPLES FOR INVESTIGATION. TEN (10) OF THE SAMPLES WERE EVALUATED BY FUNCTIONAL DRAW TESTING AND THE INDICATED FAILURE MODE FOR CLOGGED CANNULA WITH THE INCIDENT LOT WAS NOT OBSERVED AS ALL PRODUCT SPECIFICATIONS WERE MET. BASED ON A REVIEW OF THE DEVICE HISTORY RECORD FOR THE INCIDENT LOT, ALL PRODUCT SPECIFICATIONS AND REQUIREMENTS FOR LOT RELEASE WERE MET. THERE WERE NO RELATED QUALITY ISSUES DURING MANUFACTURING OF THE PRODUCT. THIS COMPLAINT IS UNABLE TO BE CONFIRMED FOR THE INDICATED FAILURE MODE CLOGGED CANNULA. BD WAS NOT ABLE TO IDENTIFY A ROOT CAUSE FOR THE INDICATED FAILURE MODE. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. OUR BUSINESS TEAM REGULARLY REVIEWS THE COLLECTED DATA FOR IDENTIFICATION OF EMERGING TRENDS."
IT WAS REPORTED WHILE USING AN UNSPECIFIED NUMBER OF BD VACUTAINER® PRECISIONGLIDE¿ MULTIPLE SAMPLE NEEDLES, THE DEVICES WERE CLOGGED, NOT ALLOWING FLUID TO PASS. THERE WAS NO REPORT OF ADVERSE IMPACT TO PATIENTS OR USERS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 226783 | BD VACUTAINER® PRECISIONGLIDE¿ MULTIPLE SAMPLE NEEDLE | BLOOD COLLECTION NEEDLE | FMI | BECTON, DICKINSON AND COMPANY (BD) | 4003277 | 30382903602101 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |