WELL LEAD MEDICAL CO. LTD recalls SunMed Tracheal Tube
- Recalling company
- WELL LEAD MEDICAL CO. LTD
- Product
- SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25
- Reason
- The 6Fr suction catheter could not pass through the samples smoothly.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jul 31, 2026
- Reported
- Sep 23, 2026
- Distribution
- US Nationwide distribution in the state of MI.
- Status
- Ongoing
- Quantity
- 27200
- Lot / codes
- 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;
- Company location
- Guangzhou, N/A
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3172-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3172-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.