Reported Apr 24, 2024 · Ongoing

Masimo Rad-G, Pulse Oximeter (W/Sensor), REF:9847, Rx Only,

Masimo Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Masimo Corporation · 52 Discovery · Irvine, CA · 92618-3105

Is this the product you have?

  • Masimo Rad-G, Pulse Oximeter (W/Sensor)
  • REF9847, Rx Only
Lot codes and dates
  • UDI(01)00843997013284/
  • Serial Numbers

    2,960 of 2,960 codes

    • 6000062119
    • 6000062120
    • 6000062121
    • 6000062122
    • 6000062123
    • 6000062124
    • 6000062125
    • 6000062126
    • 6000062127
    • 6000062128
    • 6000062129
    • 6000062130
    • 6000062131
    • 6000062132
    • 6000062133
    • 6000062134
    • 6000062135
    • 6000062136
    • 6000062137
    • 6000062138
    • 6000062139
    • 6000062140
    • 6000062141
    • 6000062142
    • 6000062143
    • 6000062144
    • 6000062145
    • 6000062146
    • 6000062147
    • 6000062148
    • 6000062149
    • 6000062150
    • 6000062151
    • 6000062152
    • 6000062153
    • 6000062154
    • 6000062155
    • 6000062156
    • 6000062157
    • 6000062158
    • 6000062159
    • 6000062160
    • 6000062161
    • 6000062162
    • 6000062163
    • 6000062164
    • 6000062165
    • 6000062166
    • 6000062167
    • 6000062168
    • 6000062169
    • 6000062170
    • 6000062171
    • 6000062172
    • 6000062173
    • 6000062174
    • 6000062175
    • 6000062176
    • 6000062177
    • 6000062178
Amount recalled
21,723 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

Why it was recalled

Their is a potential that Oximeter may automatically power off and on resulting in loss of monitoring.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:44 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.