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

Recall Z-1678-2015 — KimVent Turbo-Cleaning Closed Suction System for Adults, 10 F T-Piece (Product Code 227105); KimVent Turbo-Cleaning Closed Suction System for Adults, 12 F, DSE (Product Code 2271603); KimVent Turbo-Cleaning Closed Suction System for Adults, 12 F, T-Piece (Product Code 227135).

U.S. FDA — Device Enforcement · United States · 2015-04-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1678-2015
Date of alert: 2015-04-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Halyard Health, Inc
Product category: device
Product type: Devices

Reported risk: The internal blue flapper valve of certain KimVent Turbo-Cleaning Closed Suction System for Adults may have a potential defect. If present, the defect potentially allows air to leak out of the closed ventilator circuit.

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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