Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1429-2018 — 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;

U.S. FDA — Device Enforcement · United States · 2018-02-07 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1429-2018
Date of alert: 2018-02-07
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Halyard Health, Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 22712183

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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