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

AirLife Adult Manual Resuscitator, 40" (1.0m) Oxygen Reservoir Tubing, Adult Mask, REF 2K8005 — recall Z-1061-2024

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-1061-2024
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)
50190752114157
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.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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.