B Braun Medical Inc recalls B. Barun Hemodialysis Bloodlines
- Recalling company
- B Braun Medical Inc
- Product
- B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.
- Reason
- Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Mar 19, 2026
- Reported
- Apr 22, 2026
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
- Status
- Ongoing
- Quantity
- 328,640 units
- Lot / codes
- Model Number: SL-2000M2095L; UDI-DI Primary: 04046955348909; UDI-DI Unit: 04046955348893; All lots manufactured since 29JUN2025.
- Company location
- Bethlehem, PA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1801-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1801-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.