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

Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9849, Rx Only, — recall Z-1538-2024

U.S. FDA — Device Enforcement · United States · 2024-02-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1538-2024
Date of alert
2024-02-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Masimo Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00843997000666
Reported risk: Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring.
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.