FDA Medical devices recall ·
SunMed Tracheal Tube, Size 2.5 recall
- Recall number
- Z-3172-2026
- Date
- (initiated July 31, 2026)
- Company / brand
- Well Lead Medical CO. Ltd
NO. 47 Guomao Avenue South , Panyu, Guangzhou, N/A, China - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 27200
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25
Why was it recalled?
The 6Fr suction catheter could not pass through the samples smoothly.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
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;
Distribution
US Nationwide distribution in the state of MI.
States: Michigan
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-3172-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.