Reported Apr 24, 2024 · Ongoing

Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9849, 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/Patient Cable)
  • REF9849, Rx Only
Lot codes and dates
  • UDI(01)00843997000666/Serial
  • Number

    2,960 of 2,960 codes

    • 6000063773
    • 6000063918
    • 6000064156
    • 6000064251
    • 6000064298
    • 6000065602
    • 6000066119
    • 6000066282
    • 6000066408
    • 6000066411
    • 6000066442
    • 6000066476
    • 6000066577
    • 6000066623
    • 6000066856
    • 6000067119
    • 6000067120
    • 6000067122
    • 6000067134
    • 6000067140
    • 6000067142
    • 6000067145
    • 6000067150
    • 6000067151
    • 6000067162
    • 6000067163
    • 6000067167
    • 6000067168
    • 6000067170
    • 6000067173
    • 6000067175
    • 6000067176
    • 6000067177
    • 6000067178
    • 6000067179
    • 6000067180
    • 6000067182
    • 6000067183
    • 6000067185
    • 6000067186
    • 6000067188
    • 6000067192
    • 6000067193
    • 6000067194
    • 6000067196
    • 6000067198
    • 6000067201
    • 6000067202
    • 6000067207
    • 6000067211
    • 6000067224
    • 6000067225
    • 6000067235
    • 6000067241
    • 6000067245
    • 6000067246
    • 6000067247
    • 6000067252
    • 6000067256
    • 6000067269
    60
Amount recalled
4978 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.

Want the full recall guide?

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, 5:41 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.