8 results
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52ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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BIOPHEN Protein C 5 kit is for in vitro quantitative determination of Protein C activity on human citrated plasma. Protein C is a glycoprotein, vitamin K dependent, which inhibits coagulation. Protein C in plasma is measured following a specific activation with Protac (Agkistrodom Contortrix), an enzyme extracted from snake venom. Activated protein C hydrolysis the chromogenic substrate (SaPC-21) which release para-nitroaniline (pNA). The amount of pNA released (measured by absorbance at 405 nm) is directly proportional to the concentration of Protein C in the specimen.
FDA Recall
Open, Classified
·Aniara Diagnostica LLC·Product code GGP·February 1, 2023
ZYMUTEST HIA MonoStrip, IgGAM ELISA kit, Model No. RK041D, for in vitro diagnostic use.
FDA Recall
Terminated
·Aniara Diagnostica LLC·Product code LCO·July 19, 2019
BIOPHEN UFH Control C1, REF 224101
FDA Recall
Terminated
·Aniara Diagnostica LLC·Product code GGN·March 19, 2019
BIOPHEN UFH Control Plasma
FDA Recall
Terminated
·Aniara Diagnostica LLC·Product code GGN·June 28, 2022
BIOPHEN UFH Control C2, REF 223901
FDA Recall
Terminated
·Aniara Diagnostica LLC·Product code GGN·March 19, 2019
ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A
FDA Recall
Open, Classified
·Aniara Diagnostica LLC·Product code LCO·April 1, 2026
BIOPHEN LMWH Control C4, REF 224201
FDA Recall
Terminated
·Aniara Diagnostica LLC·Product code GGN·March 19, 2019
ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use.
FDA Recall
Terminated
·Aniara Diagnostica LLC·Product code LCO·July 19, 2019