Recall Register

INNOKAS MEDICAL OY: FDA recalls

FDA enforcement reports name INNOKAS MEDICAL OY as the recalling firm in 3 events. The events have 3 product records. The recalls started from 2014 to 2016. All the events are device recalls.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Enforcement events

3 events, newest first.

FDA enforcement events of INNOKAS MEDICAL OY
InitiatedProduct (first record)TypeClassRecordsStatus
27 Jul 2016CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care.DeviceClass II1Terminated
22 Oct 2015CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humansDeviceClass II1Terminated
3 Dec 2014VC150 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.DeviceClass II1Terminated

An event with 1 product record and a class that is not Class I has no page. It has a row in this table.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Recalling firm: The firm that the FDA record names for a recall.

Type and class

INNOKAS MEDICAL OY: events for each product type
TypeEvents
Device3
INNOKAS MEDICAL OY: events in each class
ClassEvents
Class II3
Share of the events of the firm in Class I
0%
Share of all events on the register in Class I
18%
Events with the status Ongoing
0

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Events by year

FDA enforcement events of INNOKAS MEDICAL OY, by the year that the recall started. The largest year is 2014, with 1 event.

Official channels

Cite this page

Recall Register. INNOKAS MEDICAL OY: FDA recalls. https://recallregister.com/firm/innokas-medical-oy/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
State of the firm address
N/A

The firm name is the spelling in the FDA records. A company with 2 spellings has 2 pages.

A firm with more products can have more recalls. This site does not compare one firm with a different firm. How the register is made. Report an error.

Questions

Which classes do the FDA recalls of INNOKAS MEDICAL OY have?
Class II: 3 events. The class is for the product of a recall. It is not a class of the firm.
What is the newest FDA recall of INNOKAS MEDICAL OY?
FDA event 74884, which the firm started on 27 Jul 2016. The first product in the record is: CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care.
How many FDA recalls of INNOKAS MEDICAL OY have the status Ongoing?
No event has the status Ongoing in the openFDA file. openFDA says about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.