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

Recall Z-2714-2014 — Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Ypiece.

U.S. FDA — Device Enforcement · United States · 2014-09-08 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2714-2014
Date of alert: 2014-09-08
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Teleflex Medical
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 0241300618

Reported risk: The pediatric breathing circuits can crack prior to and 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-2714-2014 — Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Ypiece.

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