Bubble Sensor For 3/8" X 3/32" Tubing; Model Number: 701055720;

Recall Summary A Bubble Sensor for 3/8" x 3/32" tubing (Model 701055720) is being recalled due to a durability problem with the connecting cable near where it attaches to the sensor. If the cable is bent excessively, it can break completely or lose contact, causing error messages on connected medical devices. These errors may appear temporarily when the cable moves or become permanent if the connection is fully damaged.

Recalling firm

Maquet Cardiopulmonary Gmbh Kehler Str. 31 Rastatt Germany

Product

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.

Classification

Class II

Category

consumer product recall

Country

United States

Agency

FDA-DEVICES

Recall date

2026-01-09

Status

Open, Classified

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/744c84f1-46c7-40a9-b2f2-25d54851b76a