# FDA recall Z-3172-2026

> **WELL LEAD MEDICAL CO. LTD** · Class II · device recall initiated 2026-07-31.

## Product

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

## Reason for recall

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

## Distribution

US Nationwide distribution in the state of MI.

## Key facts

- **Recall number:** Z-3172-2026
- **Recalling firm:** WELL LEAD MEDICAL CO. LTD
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-31
- **Report date:** 2026-09-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Guangzhou, N/A, China

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3172-2026

## Citation

> MORVS. FDA recall Z-3172-2026. Retrieved 2026-10-16 from https://api.morvs.ai/recall/Z-3172-2026. Source: US FDA. Licensed CC0.

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