Recall Z-3172-2026

Well Lead Medical Co. Ltd · initiated July 31, 2026

Open, Classified

Product

SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25

Codes / lots: 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;

Reason for recall

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

FDA-determined cause: Process control

Action taken

On July 31, 2026 URGENT: MEDICAL DEVICE RECALL letters were emailed to customers. Actions to be taken: 1. We request that you check your inventory for product within the scope of this recall. Quarantine all impacted product immediately. Cease use and distribution immediately. 2. If the affected product is currently in use on a patient, do not perform a prophylactic endotracheal tube exchange solely due to this notification. Continue to manage the patient according to institutional protocols and clinical judgment. 3. If you do have stock in scope of this recall, mark the applicable checkbox on the Affected Product Information Table and contact Well Lead by E-mail . 4. If you do not have stock in scope of this recall, mark the applicable checkbox on the Affected Product Information Table and return the form to the E-mail address . 5. For affected products, please contact your distributor to arrange product replacement.

Details

Recall number
Z-3172-2026
Initiated
July 31, 2026
Posted by FDA
September 15, 2026
Product code
BTR – Tube, Tracheal (W/Wo Connector)
Quantity
27200
Distribution
US Nationwide distribution in the state of MI.
Recalling firm
Well Lead Medical Co. Ltd, Guangzhou

Official FDA recall record