BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE
Report
- Report Number
- 1917413-2026-00412
- Event Type
- Malfunction
- Date Received
- May 11, 2026
- Date of Event
- April 13, 2026
- Report Date
- April 16, 2026
- Manufacturer
- BECTON DICKINSON & CO (FRANKLIN LAKES)
- Product Code
- JCF
- UDI-DI
- 30382903627616
- PMA / PMN Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AZ, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
B3: DATE OF EVENT IS UNKNOWN. THE DATE RECEIVED BY MANUFACTURER HAS BEEN USED FOR THIS FIELD. INVESTIGATION SUMMARY: BD DID NOT RECEIVE ANY SAMPLES FOR INVESTIGATION. A TOTAL OF 60 RETAINED SAMPLES FROM LOT 5344609 AND 5196721 AND 55 RETAINED SAMPLES FROM LOT 5230375 WERE VISUALLY INSPECTED, WITH NO ISSUES IDENTIFIED. BASED ON A REVIEW OF THE DEVICE HISTORY RECORD FOR THE INCIDENT LOTS, ALL PRODUCT SPECIFICATIONS AND REQUIREMENTS FOR LOT RELEASE WERE MET. THIS COMPLAINT HAS NOT BEEN CONFIRMED FOR THE LOTS 5196721, 5230375 AND 5344609, FOR THE INDICATED FAILURE MODE: DAMAGED. 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. THE BUSINESS TEAM REGULARLY REVIEWS THE COLLECTED DATA FOR THE IDENTIFICATION OF EMERGING TRENDS.
REPORT 2 OF 3: IT WAS REPORTED WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, 1 TUBE CRACKED CLEANLY DURING CENTRIFUGATION AND CHIPS WERE NOTED IN THE LIP OF THE TUBE. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 70256 | BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE | LYMPHOCYTE SEPARATION MEDIUM | JCF | BECTON DICKINSON & CO (FRANKLIN LAKES) | 5196721 | 30382903627616 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |