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

Recall Z-0866-2015 — KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.

U.S. FDA — Device Enforcement · United States · 2014-11-17 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0866-2015
Date of alert: 2014-11-17
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Halyard Health
Product category: device
Product type: Devices

Reported risk: The cuff inflation line may detach from the endotracheal tube 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.

Recall Z-0866-2015 — KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.

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