Fresh Recalls

WELL LEAD MEDICAL CO recalls

Recall found. WELL LEAD MEDICAL CO is named in FDA Class II recall Z-3172-2026 covering SunMed Tracheal Tube. Hazard: The 6Fr suction catheter could not pass through the samples smoothly. Identifying details: 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;. Status: Ongoing.

Models with recalls

SunMed Tracheal Tube (1)

All WELL LEAD MEDICAL CO recalls

FDA Class II · Medical device · September 23, 2026

SunMed Tracheal Tube recall — WELL LEAD MEDICAL CO. LTD

The 6Fr suction catheter could not pass through the samples smoothly.

Official ID Z-3172-2026 · Official record ↗

Verify with the official sources:

Found something wrong or missing? Report a data error.

Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.