device recall
saveMaquet Cardiopulmonary Gmbh device recall (Cls II)
January 9, 2026updated 3mo ago
community read0 votes
Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720; — Reason: 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. — Status: Ongoing
view source ↗
comments(0)
5-min edit window · permanent after that