FDAJanuary 9, 2026device

Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending of the connecting cable can lead to full damage of the Venous Bubble Sensor or loose cable contact, which may trigger the errors Ven. bubble sensor defective or Ven. bubble sensor disconnected on the connected medical device. These errors can occur temporarily when the connecting cable is moved or permanently if the connection is fully compromised.

What to do

FDA enforcement status: Ongoing

Brands named

maquet cardiopulmonarymaquet

UPCs

04037691816432

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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