Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CARESCAPE VC150 Vital Signs Monitor Recalled by INNOKAS MEDICAL OY Due to A software error on released software versions 1.6.12,...
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
CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care.
Quantity: 1715 units
Why Was This Recalled?
A software error on released software versions 1.6.12, 1.6.12F and 1.6.16 may give wrong time data to measurements.
Where Was This Sold?
This product was distributed to 15 states: AZ, AR, FL, IN, LA, MA, MI, NJ, NM, NY, NC, OH, PA, TN, WI
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