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

Recall Z-1399-2017 — Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker Endo-Bronch with Flex Tip). Model Numbers: H-PFTDL-28-1, H-PFTDL-32-1, H-PFTDL-35-1, H-PFTDL-37-1, H-PFTDL-39-1, H-PFTDL-41-1. The product is an endotracheal tube with a double lumen for single lung isolation allowing for ven

U.S. FDA — Device Enforcement · United States · 2016-12-16 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1399-2017
Date of alert: 2016-12-16
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Parker Medical
Product category: device
Product type: Devices

Reported risk: The product was not functioning as intended. The ventilation to the patient was not disrupted, but the single lung isolation and ventilation did not function as intended.

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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