Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | ongoing |
| Recall date | January 09, 2026 |
| Reported | February 11, 2026 |
| Recalling firm | Maquet Cardiopulmonary Gmbh |
| Country / region | Germany N/A |
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.
Affected products
- Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
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