Class II — Potential Health Hazard

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,...

Date: July 27, 2016
Company: INNOKAS MEDICAL OY
Status: Terminated
Source: FDA (Device)

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

Affected (15 states)Not affected

About INNOKAS MEDICAL OY

INNOKAS MEDICAL OY has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report