ClearanceBrief
Recall Z-1530-2014 ยท CIT Nadh Oxidation/Nad Reduction, Ast/Sgot

Alfa Wassermann, Inc.

Alfa Wassermann Diagnostic Technologies, LLC. ACE AST Reagent. Product Usage: For quantitative determination of AST in serum and lithium heparin plasma using ACE, ACE Alera and ACE Axcel Clinical Chemistry Systems. This test is intended for use in clinical laboratories and physician office laboratories.

DateApr 30, 2014 (initiated Mar 5, 2014)
StatusTerminated
ReasonExtremely low absorbance readings.
Root causeProcess control
ActionAlfa Wassermann Diagnostic Technologies, LLC issued an "Important: Advisory Notice/"Product Response Form" dated March 5, 2014 and sent on March 6, 2014 to their customers for ACE ALT Reagent Product reorder number SA1046 Lot F3604. They issued a follow-up "Important: Advisory Notice/"Product Response Form" dated March 21, 2014 and sent on March 26, 2014 to their customers for ACE AST Reagent Product reorder numbers SA1047, Lot F3609, and RX1047, Lot F3610. The notification identified the product(s), problem, and actions to be taken by the customers. Customers were instructed to destroy any
QuantitySA1047 lot F3609: 146; RX1047 lot F3610: 53
DistributionUS Nationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K113382ACE ALT REAGENT
Alfa Wassermann, Jul 19, 2012