FDA recall record

Medtest Holdings Pointe Scientific Liquid Creatine Kinase Reagent Set Device is a kit recall — FDA Z-2650-2017

Linear performance information in product insert does not match that listed in the approved premarket notification

Class IIIclassification
Z-2650-2017official record ID
Jul 5, 2017report date

Recall record at a glance

Official recordZ-2650-2017
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmMedtest Holdings, Inc.
Report dateJul 5, 2017
Recall initiation dateOct 19, 2011
Quantity319.922 L
LocationCanton, MI, United States

Official product description

Pointe Scientific Liquid Creatine Kinase Reagent Set Device is a kit comprised of two reagents an R 1 Buffer and R2 CK enzyme solution. Intended Use: For the kinetic quantitative determination of creatine kinase activity in serum.

Why the product was recalled

Linear performance information in product insert does not match that listed in the approved premarket notification

Distribution information

Nationwide Distribution

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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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