FDAFDA · Food and drugs·Recall number Z-3172-2026
SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25
Published September 23, 2026 · Recall initiated: July 31, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The 6Fr suction catheter could not pass through the samples smoothly.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- WELL LEAD MEDICAL CO. LTD
- Distributor
- US Nationwide distribution in the state of MI.
- Lot
- Model Number: 1-7333-25; UDI-DI:10889483048108; Lot No.: 2108011462, 2108011506, 2109011963, 2111012039, 2112012040, 2204010568, 2204010569, 2204010734, 2205010833, 2207011263, 2208011729, 2208011789, 2304010830, 2306011372, 2306011425, 2308011907, 2308012011, 2308012012, 2309012128, 2310012358, 2310012599, 2311013016, 2311012924, 2312013223, 2401010069, 2401010197, 2402010378, 2403010466, 2403010889, 2404010999, 2406011822, 2407012282, 2408012389, 2409012800, 2409012882, 2508013006, 2510013653, 2511014081, 2512014080, 2602010272, 2603010274, 2603010900, 2604011014, 2604011416, 2605011923, 2605011924;
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- China
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