B. Braun StreamLine long bloodlines may accumulate arterial air bubbles
B. Braun is recalling StreamLine Bloodline Long Version sets because small air bubbles can accumulate in the arterial line under negative pressure. 328,640 units are affected.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: FDA Class I recall, which the rubric floors at Severe; no death is reported in the source, so it does not escalate to Critical.
Plain-English summary
B. Braun is recalling Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC, model number SL-2000M2095L, primary UDI-DI 04046955348909. The action covers 328,640 units and applies to all lots manufactured since 29 June 2025.
The recall is due to the potential for the accumulation of small air bubbles in the arterial line, caused by the adherence of blood gases to the tubing under negative pressure. The FDA classified the action as Class I, its most serious classification.
Distribution was worldwide, covering the United States nationwide and Canada. The bloodlines are supplied to dialysis facilities rather than sold to consumers.
Facilities should identify affected stock using the model number and UDI-DI above, quarantine it, and follow the instructions issued by B. Braun.
The recalled product
- Product
- B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.
- Manufacturer
- B Braun Medical Inc
- Affected units
- 328,640
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Model Number: SL-2000M2095L
- UDI-DI Primary: 04046955348909
- UDI-DI Unit: 04046955348893
- All lots manufactured since 29JUN2025.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 6 recalled by B Braun Medical Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 6 products in this recall →Related recalls
Same manufacturer · B Braun Medical Inc
See all →- LowB Braun Recalls Discofix Stopcock Sets Due to Incorrect Expiration Date
FDA (Devices) · 2026-09-09
- SevereB. Braun Recalls Lactated Ringer's Injection Due to Particulate Matter
FDA (Drugs) · 2026-09-02
- SevereDesign Options spinal trays recalled over Huons bupivacaine quality issues
FDA (Devices) · 2026-06-10
- ModerateB. Braun Shands kits contain Mastisol adhesive with cracking tubing
FDA (Devices) · 2026-06-10
- ModerateB. Braun spinal epidural kits contain Mastisol with cracking tubing
FDA (Devices) · 2026-06-10
Same hazard · air embolism risk
See all →- SevereCoronary angio packs recalled over Medline syringe rotating adaptor defect
FDA (Devices) · 2026-05-13
- SevereB. Braun 4.8 mm hemodialysis bloodlines may accumulate arterial air bubbles
FDA (Devices) · 2026-04-22
- SevereB. Braun StreamLine Dialog DR bloodlines may accumulate arterial air bubbles
FDA (Devices) · 2026-04-22
- SevereB. Braun StreamLine Fresenius bloodlines may accumulate arterial air bubbles
FDA (Devices) · 2026-04-22
- SevereB. Braun hemodialysis bloodlines may accumulate air bubbles in the arterial line
FDA (Devices) · 2026-04-22