FDA recall record

B Braun Medical B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT recall — FDA Z-1803-2026

Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.

Class Iclassification
Z-1803-2026official record ID
Apr 22, 2026report date

Recall record at a glance

Official recordZ-1803-2026
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmB Braun Medical Inc
Report dateApr 22, 2026
Recall initiation dateMar 19, 2026
Quantity4,884 units
LocationBethlehem, PA, United States

Official product description

B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.

Why the product was 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.

Distribution information

Worldwide distribution - US Nationwide and the country of Canada.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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