# FDA recall Z-1429-2018

> **Halyard Health, Inc** · Class II · device recall initiated 2018-02-07.

## Product

Halyard Closed Suction System for Adults, Multi-Access¿Port¿Closed¿Suction¿System¿for¿Adults.  Used to aspirate liquids or semisolids from a patient's upper airway.      a. HALYARD* MULTI-PORT, DSY, ENDO 10FR;    b. HALYARD* MULTI-PORT, DSY, ENDO 12FR;    c. HALYARD* MULTI-PORT, DSY, ENDO, MDI 12FR;    d. HALYARD* MULTI-PORT, DSY, ENDO 14FR;    e. HALYARD* MULTI-PORT, DSY, TRACH 14FR;    f. HALYARD* MULTI-PORT, DSY, TRACH, WP 14FR;    g. HALYARD* MULTI-PORT, DSY, ENDO, MDI 14FR;    h. HALYARD* MULTI-PORT, DSY, ENDO, WP 14FR;    i. HALYARD* MULTI-PORT, DSY, ENDO, WP 14FR;    j. HALYARD* MULTI-PORT, DSY, ENDO, MDI 14FR;    k. HALYARD* MULTI-PORT, DSY, ENDO, MDI 16FR;

## Reason for recall

Certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex Connector may become loose or disconnect before use or during use.

## Distribution

Worldwide distribution.  US nationwide including Puerto Rico, ARGENTINA, AUSTRALIA, BAHAMAS, BELGIUM, BOLIVIA, BRAZIL, BULGARIA, CANADA, CHILE, CHINA, COLOMBIA, COSTA RICA, CROATIA, CZECH REPUBLIC, DOMINICAN REP., ECUADOR, EL SALVADOR, GUATEMALA, HONG KONG, HUNGARY, INDIA, IRELAND, ISRAEL, ITALY, JAPAN, JORDAN, KAZAKHSTAN, LEBANON, MALAYSIA, MEXICO, NEW ZEALAND, PERU, PHILIPPINES, QATAR, ROMANIA, RUSSIAN FEDERATION, SAUDI ARABIA, SINGAPORE, SLOVENIA, SOUTH AFRICA, SOUTH KOREA, SPAIN, SWEDEN, THAILAND, UNITED KINGDOM, and UNITED ARAB EMIRATES.

## Key facts

- **Recall number:** Z-1429-2018
- **Recalling firm:** Halyard Health, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-02-07
- **Report date:** 2018-04-25
- **Termination date:** 2022-01-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Alpharetta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1429-2018

## Citation

> AI Analytics. FDA recall Z-1429-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1429-2018. Source: US FDA. Licensed CC0.

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