Use caution Medical device recall · FDA · Published September 30, 2025

B. Braun Hemodialysis Bloodline Set Recall: Micro-air Bubbles Risk

B. Braun recalls STREAMLINE BLOODLINE SET FOR DIALOG (model SL-2010M2096) due to potential micro-air bubbles in bloodlines causing alarm errors. Affected units include specific lot numbers listed in the recall.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0070-2026Medical device B. Braun ›

Use caution until it’s fixed

The potential for micro-air bubbles observed in the bloodline and air-in-line alarms due to damaged arterial and venous patient connectors.

Take action

Contact the company

Recalling firmB BRAUN MEDICAL INC861 Marcon Blvd · Allentown, PA 18109-9577

✎ GovInfoNow plain-language explainer

B. Braun is recalling certain hemodialysis bloodline sets that may have damaged connectors, potentially causing micro-air bubbles in the bloodline and air-in-line alarms. This could lead to inaccurate alarms during dialysis treatments, which is a serious risk for patients. Read more at govinfonow.com/recall/51162-b-braun-hemodialysis-bloodline-set-recall-micro-air-bubbles-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/51162-b-braun-hemodialysis-bloodline-set-recall-micro-air-bubbles-risk · Updated August 17, 2026 · FDA enforcement record: FDA #Z-0070-2026

Cite this page

“B. Braun Hemodialysis Bloodline Set Recall: Micro-air Bubbles Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51162-b-braun-hemodialysis-bloodline-set-recall-micro-air-bubbles-risk. Based on FDA recall #Z-0070-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0070-2026%22&limit=1).

B. Braun Medical Inc. recalled STREAMLINE BLOODLINE SET FOR DIALOG hemodialysis bloodlines due to the potential for micro-air bubbles and alarm failures caused by damaged connectors, the FDA said on Sept. 30, 2025.

How to tell if you have it

Brand: B. Braun
Product Name: STREAMLINE BLOODLINE SET FOR DIALOG
Model/Catalog Number: SL-2010M2096
Lot Numbers: A2500119, A2500121, A2500128, A2500129, A2500130, A2500132, A2500133, A2500134, A2500149, A2500150, A2500151, A2500180, A2500181, A2500182, A2500185, A2500198, A2500199, A2500200, A2500203, A2500204, A2500205, A2500206, A2500207, A2500208, A2500209, A2500210, A2500211, A2500212, A2500213, A2500214, A2500215, A2500216, A2500217, A2500218, A2500219, A2500220, A2500246, A2500247, A2500248, A2500249, A2500250, A2500251, A2500257, A2500258, A2500259, A2500260, A2500261, A2500262, A2500267, A2500268, A2500269, A2500273, A2500274, A2500275, A2500276, A2500277, A2500278, A2500295, A2500298, A2500299, A2500300, A2500318, A2500319, A2500320, A2500321, A2500322, A2500323, A2500324, A2500325, A2500326, A2500327, A2500328, A2500329, A2500330, A2500356, A2500357
Distribution: US Nationwide

The hazard

The recall addresses the potential for micro-air bubbles observed in the bloodline and air-in-line alarms due to damaged arterial and venous patient connectors. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show B Braun Medical Inc has 66 other recalls on record since 2013-10-15. Recent brand recalls include a 2026-08-19 Sodium Chloride Injection recall for particulate matter, a 2026-08-12 Lactated Ringer's Injection recall for particulate matter, and a 2026-08-04 Discofix Four Way Stopcock recall for an incorrect expiration date. Other recent recalls of similar products include a 2026-08-10 Fresenius Medical Care 5008X Blood Tubing Set recall for risk of blood leak and a 2025-10-27 Medline Perfusion Syringe recall for potential sensitization risk.

How to tell if you have this one

Check for the model number SL-2010M2096 on the product. Affected units include specific lot numbers listed in the recall notice, such as A2500119 through A2500357.

Brand
B. Braun
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the model number (SL-2010M2096) and lot numbers on the bloodline set.
Contact Manufacturer
Reach out to B. Braun Medical Inc for guidance on whether your specific unit is affected and next steps.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Domestic: US Nationwide Distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 29 days after the firm started it.

Sep 30, 2025Firm started the recall
Oct 22, 2025FDA classified it Class I
Oct 29, 2025Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/51162-b-braun-hemodialysis-bloodline-set-recall-micro-air-bubbles-risk">B. Braun Hemodialysis Bloodline Set Recall: Micro-air Bubbles Risk (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0070-2026 (September 30, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0070-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.