Drug recall
Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
FDA recall event 98159 · Class II · Maquet Cardiopulmonary Gmbh
Key facts
| Event ID | 98159 |
|---|---|
| Recall numbers | Z-1300-2026 |
| Recalling firm | Maquet Cardiopulmonary Gmbh |
| Product type | Devices |
| Products | Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720; |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Jan 9, 2026 |
| Report date | Feb 11, 2026 |
| City | Rastatt |
| Country | Germany |
| FEI number | 3009507273 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: