Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VC150 Vital Signs Monitor (VC150 monitor equipped with Masimo SpO2 Recalled by INNOKAS MEDICAL OY Due to If the SpO2 or RRa value is violating...
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 INNOKAS MEDICAL OY directly.
Affected Products
VC150 Vital Signs Monitor (VC150 monitor equipped with Masimo SpO2 technique only); Innokas Medical CARESCAPE VC150 Rx Only Innokas Medical Oy. Catalog numbers 2067980-002, 2067980-006, 2067980-010, and 2067980-014.
Quantity: 20 units
Why Was This Recalled?
If the SpO2 or RRa value is violating the respective alarm limit at the time of switching to monitoring mode, the monitor does not issue visual and audible alarms.
Where Was This Sold?
Distributed in the US and Europe.
About INNOKAS MEDICAL OY
INNOKAS MEDICAL OY has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report