FDA Device recall Z-1429-2018
Halyard Closed Suction System for Adults, Multi-Access¿Port¿Closed¿Suction¿System¿for¿Adults
- FDA Device
- Class II
- terminated
- Published 2018-04-25
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
| Agency | FDA Device |
|---|---|
| Recall number | Z-1429-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-07 |
| Published | 2018-04-25 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Halyard Health |
| Distribution | US |
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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