FDA recall record

INNOKAS MEDICAL OY CARESCAPE VC150 Vital Signs Monitor recall — FDA Z-2604-2016

A software error on released software versions 1.6.12, 1.6.12F and 1.6.16 may give wrong time data to measurements.

Class IIclassification
Z-2604-2016official record ID
Aug 31, 2016report date

Recall record at a glance

Official recordZ-2604-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmINNOKAS MEDICAL OY
Report dateAug 31, 2016
Recall initiation dateJul 27, 2016
Quantity1715 units
LocationKEMPELE, Finland

Official product description

CARESCAPE VC150 Vital Signs Monitor; Intended to monitor a single patient's vital signs at the site of care.

Why the product was 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.

Distribution information

AR, AZ, FL, IN, LA, MA, MI, NC, NJ, NM, NY, OH, PA, TN, WI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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