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RAD-G 9210Recalls & reported problems

Masimo Corporation · Rad-G, Temp, with sensor · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

1 other recall cover devices cleared under the same FDA submission (K213676); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Feb 15, 2024Open, Classified

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

    Z-1536-2024 · Root cause: Material/Component Contamination · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K213676. One submission often covers many models, so check the product and lot details in each record.

  • Z-1539-2024 · Feb 15, 2024 · Open, Classified
    Masimo Rad-G, Pulse Oximeter (W/Patient Cable), REF:9895 Rx Only,

Other Oximeter devices

All Oximeter devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.