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

Recall Z-1060-2024 — AirLife Adult Manual Resuscitator, Oxygen Reservoir Bag, Adult Mask, CO2 Detector, REF 2K8004C2

U.S. FDA — Device Enforcement · United States · 2024-01-10 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1060-2024
Date of alert
2024-01-10
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Vyaire Medical
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
50190752114119
Reported risk: Risk of hypoventilation caused by duckbill and ring broken/disassembled, due to faulty mold/tooling producing out of specification components. Device failure may cause improper ventilation or no ventilation that may result in hypoventilation or hypoxia, and potentially lead to death. The mold/tooling used to produce the affected component was replaced in 2017.
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.