HEMODIALYSIS BLOODLINES
Report
- Report Number
- 2521402-2025-01189
- Event Type
- Malfunction
- Date Received
- October 22, 2025
- Date of Event
- September 24, 2025
- Report Date
- February 16, 2026
- Manufacturer
- B. BRAUN MEDICAL INC.
- Product Code
- FJK
- UDI-DI
- 04046964367786
- PMA / PMN Number
- K080807
- Removal / Correction Number
- Z-0070-2026
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NJ, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
THIS REPORT HAS BEEN IDENTIFIED AS B. BRAUN MEDICAL INTERNAL REPORT NUMBER (B)(4). NO SAMPLE AND/OR LOT NUMBER WAS PROVIDED FOR EVALUATION; HOWEVER, B. BRAUN MEDICAL INC. (BBMI) HAS ISSUED A VOLUNTARY URGENT FIELD SAFETY CORRECTION FOR STREAMLINE® BLOODLINE SET FOR DIALOG+® HEMODIALYSIS SYSTEM (2521402-9/3/25-004-C [Z-0070-2026]). WE WILL MAINTAIN THIS REPORT FOR FURTHER REFERENCES AND CONTINUE TO MONITOR OTHER REPORTS FOR SIMILAR OCCURRENCES. IF ANY ADDITIONAL PERTINENT INFORMATION BECOMES AVAILABLE, A FOLLOW UP WILL BE SUBMITTED.
THIS REPORT HAS BEEN IDENTIFIED AS B. BRAUN MEDICAL INTERNAL REPORT NUMBER (B)(4). THE INVESTIGATION IS ONGOING AT THIS TIME. A FOLLOW-UP WILL BE SUBMITTED WHEN THE INVESTIGATION RESULTS BECOME AVAILABLE. NOTE: LOT NUMBER PROVIDED WAS A250021. THIS NUMBER DOES NOT VALIDATE IN THE SAP SYSTEM. LOT NUMBER LISTED AS UNKNOWN IN THIS REPORT UNTIL MORE INFORMATION IS PROVIDED.
AS REPORTED BY THE USER FACILITY: REASON OF COMPLAINT: OBSERVED 3 BLOOD LINES IN ONE LOT TO HAVE MICRO BUBBLES AT ARTERIAL ACCESS CONNECTION. USED DIFFERENT LOT NUMBER AND OBSERVED THE SAME. SECOND LOT NUMBER WAS A250021.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 222650 | HEMODIALYSIS BLOODLINES | SET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE | FJK | B. BRAUN MEDICAL INC. | 04046964367786 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |