Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
rainbow Reusable Sensors. RAINBOW DCI-DC3 Recalled by Masimo Corporation Due to These sensors were manufactured with incompatible configurations. This...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Masimo Corporation directly.
Affected Products
rainbow Reusable Sensors. RAINBOW DCI-DC3, SpO2/SpCO/SpMet, Part No. 2201; RAINBOW DCI-dc8, SpO2/SpCO/SpMet, Part No. 2407; RAINBOW DCI, SpO2/SpCO/SpMet, Part No. 2696; RAINBOW DCIP, PED, SpO2/SpCO/SpMet, Part No. 2697. rainbow reusable sensors are indicated for spot check or continuous non-invasive monitoring of arterial saturation (SpO2), arterial carboxyhemoglobin saturation (SpCO), arterial methemoglobin (SpMet), and pulse rate.
Quantity: 3476 units total (3322 units in US)
Why Was This Recalled?
These sensors were manufactured with incompatible configurations. This could result in sensors that will provide either no readings or inaccurate readings for the SpCO and SpMet parameters.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Masimo Corporation
Masimo Corporation has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report