Reported Apr 24, 2024 · Ongoing

Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9895 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)
  • REF9895 Rx Only
Lot codes and dates
  • UDI(01)00843997013789/
  • Serial Numbers

    65 of 65 codes

    • 6000083849
    • 6000083870
    • 6000083875
    • 6000083898
    • 6000083909
    • 6000083932
    • 6000083941
    • 6000083959
    • 6000083974
    • 6000083978
    • 6000083983
    • 6000083991
    • 6000083997
    • 6000083999
    • 6000084011
    • 6000084018
    • 6000084020
    • 6000084042
    • 6000084055
    • 6000084075
    • 6000084084
    • 6000084090
    • 6000084101
    • 6000084106
    • 6000084112
    • 6000084132
    • 6000084133
    • 6000084157
    • 6000084163
    • 6000084181
    • 6000084205
    • 6000084211
    • 6000084222
    • 6000084236
    • 6000084276
    • 6000084290
    • 6000084364
    • 6000084392
    • 6000084394
    • 6000084429
    • 6000084439
    • 6000084442
    • 6000084454
    • 6000084455
    • 6000084457
    • 6000084513
    • 6000084536
    • 6000084543
    • 6000084567
    • 6000084574
    • 6000084575
    • 6000084607
    • 6000084613
    • 6000084647
    • 6000090319
    • 6000090325
    • 6000090331
    • 6000090333
    • 6000090339
    • 6000084465
Amount recalled
65

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, 6:20 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.