Reported Feb 11, 2026 · Ongoing
Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
Maquet Cardiopulmonary GmbH
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Maquet Cardiopulmonary Gmbh · Kehler Str. 31 · Rastatt, N/A · N/A
Is this the product you have?
- Bubble Sensor for 3/8" x 3/32" tubing
- Model Number701055720
- Lot codes and dates
- Model Number701055720
- UDI-DI04037691816432
- Serial NumbersAll units impacted
- Amount recalled
- 3050 units
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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