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

Recall Z-1231-2014 — Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated with oral endobronchial tubes, including, but not limited to, thoracic surgery, bronchospirometry, administration of endobronchial anesthesia, etc. The endobronchial tube allows v

U.S. FDA — Device Enforcement · United States · 2014-02-28 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1231-2014
Date of alert: 2014-02-28
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Teleflex Medical
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 116200260

Reported risk: The product may fail to achieve seal of right lung due to the cuff inflating to one side

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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