Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Bubble Sensor for 3/8" x 3/32" tubing Recalled by Maquet Cardiopulmonary Gmbh Due to Internal investigations have identified an issue with the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Maquet Cardiopulmonary Gmbh directly.
Affected Products
Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
Quantity: 3050 units
Why Was This 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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Maquet Cardiopulmonary Gmbh
Maquet Cardiopulmonary Gmbh has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report