RecallRadar

FDA Device recall Z-1429-2018

Halyard Closed Suction System for Adults, Multi-Access¿Port¿Closed¿Suction¿System¿for¿Adults

On 2018-04-25 the FDA classified a Class II recall of Halyard Closed Suction System for Adults, Multi-Access¿Port¿Closed¿Suction¿System¿for¿Adults by Halyard Health, citing certain Flex Connectors supplied with Halyard Closed Suction Kits with Flex Connector may become loose or disconnect before use or during use.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1429-2018
ClassificationClass II
Statusterminated
Initiated2018-02-07
Published2018-04-25
Last updated2026-09-13 11:54 UTC
CompanyHalyard Health
DistributionUS

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

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

Identifiers

code_info
Product Description, Product code: a. HALYARD* MULTI-PORT, DSY, ENDO 10FR, 24010-5; b. HALYARD* MULTI-PORT, DSY…Product Description, Product code: a. HALYARD* MULTI-PORT, DSY, ENDO 10FR, 24010-5; b. HALYARD* MULTI-PORT, DSY, ENDO 12FR, 240121-5; c. HALYARD* MULTI-PORT, DSY, ENDO, MDI 12FR, 240128-5; d. HALYARD* MULTI-PORT, DSY, ENDO 14FR, 24014-5; e. HALYARD* MULTI-PORT, DSY, TRACH 14FR, 240143-5; f. HALYARD* MULTI-PORT, DSY, TRACH, WP 14FR, 2401436-5; g. HALYARD* MULTI-PORT, DSY, ENDO, MDI 14FR, 2401438-5; h. HALYARD* MULTI-PORT, DSY, ENDO, WP 14FR, 240146-5; i. HALYARD* MULTI-PORT, DSY, ENDO, WP 14FR, 240146-5N; j. HALYARD* MULTI-PORT, DSY, ENDO, MDI 14FR, 240148-5; k. HALYARD* MULTI-PORT, DSY, ENDO, MDI 16FR, 240168-5; j. HALYARD* TRACH CARE-72 DSE MDI BUILT IN ENDO 10FR, 2271018-5; k. HALYARD* TRACH CARE-72 DSE MDI BUILT IN ENDO 12FR, 2271218-5; l. HALYARD* TURBO-CLEANING 12FR DSE 12IN/30.5CM (WHITE), 22712183; m. HALYARD* 72 DSE MDI BUILT IN ENDO 12FR, 22712186-5; n. HALYARD* 72 DSE TRACH CARE 12FR, 227121863-5; o. HALYARD* 14FR DSE 22.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1429-2018%22

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