Drug recall
SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25
FDA recall event 99685 · Class II · WELL LEAD MEDICAL CO. LTD
Key facts
| Event ID | 99685 |
|---|---|
| Recall numbers | Z-3172-2026 |
| Recalling firm | WELL LEAD MEDICAL CO. LTD |
| Product type | Devices |
| Products | SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The 6Fr suction catheter could not pass through the samples smoothly. |
| Initiation date | Jul 31, 2026 |
| Report date | Sep 23, 2026 |
| City | Guangzhou |
| Country | China |
| FEI number | 3010400865 |
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: