B. Barun Hemodialysis Bloodlines recall
B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.
Why was B. Barun Hemodialysis Bloodlines recalled?
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model Number: SL-2000M2095L; UDI-DI Primary: 04046955348909; UDI-DI Unit: 04046955348893; All lots manufactured since 29JUN2025.
- Product
- B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.
- Recalling firm
- B Braun Medical Inc
- Quantity
- 328,640 units
- Distribution
- Worldwide distribution - US Nationwide and the country of Canada.
- Recall date
- April 22, 2026
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)