medical Class II Updated 2018-09-26

Polymedco, Inc.,/Polymedco Cancer Diagnostic Products, Llc recalls PATHFAST NTproBNP Catalog Number: PF1061-KUS PATHFAST¿

Recalled Product

PATHFAST NTproBNP Catalog Number: PF1061-KUS PATHFAST¿ NTproBNP is a product for in-vitro diagnostic use with the in vitro diagnostic system PATHFAST¿ for the quantitative measurement of N-terminal-pro B-type Natriuretic Peptide (NT-proBNP) in heparinized or EDTA whole blood and plasma.


Hazard / Issue

A pinhole caused by the laser printer in the aluminum sheet over the ALP reagent wells caused leakage through the pinhole. If the cartridge with leakage is used, higher measurement value as low as +12% and no higher than +20% bias may be obtained.

Issued by

FDA

Affected States: AR, CA, FL, ID, LA, MN, NY, TX
Lot/Code Info: Lot : A735 Exp: 10/31/2018 UDI: (01)04987595301636(17)181031(10)A735 and Lot: O736 Exp: 01/03/2019 UDI: (01)04987595301636(17)190131(10)O736
View official government recall

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →