# FDA recall Z-0143-2025

> **Smiths Medical ASD Inc.** · Class II · device recall initiated 2024-07-18.

## Product

smiths medical portex, Nasopharyngeal Airway, Sizes as follows:    a)	AIRWAY NASOPHARYNGEAL 6.0MM, REF 100/210/060;   b)	AIRWAY NASOPHARYNGEAL 6.0MM, REF 100/210/060JP;   c)	AIRWAY NASOPHARYNGEAL 7.0MM, REF 100/210/070;   d)	AIRWAY NASOPHARYNGEAL 7.0MM, REF 100/210/070JP;   e)	AIRWAY NASOPHARYNGEAL 8.0MM, REF 100/210/080;   f)	AIRWAY NASOPHARYNGEAL 8.0MM, REF 100/210/080JP;   g)	AIRWAY NASOPHARYNGEAL 8.0MM, REF 100/210/080JS;   h)	AIRWAY NASOPHARYNGEAL 9.0MM, REF 100/210/090;   i)	AIRWAY NASOPHARYNGEAL 9.0MM, REF 100/210/090JP;

## Reason for recall

Uncertainty in the seal integrity of the sterile packaging.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-0143-2025
- **Recalling firm:** Smiths Medical ASD Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-18
- **Report date:** 2024-10-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Minneapolis, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0143-2025

## Citation

> AI Analytics. FDA recall Z-0143-2025. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0143-2025. Source: US FDA. Licensed CC0.

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