Recall Z-0741-2016

Horiba Instruments Inc · initiated January 11, 2016

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

ABX PENTRA Lactic Acid CP ref. A11A01721 reagent is intended for the quantitative in vitro diagnostic determination of lactic acid in plasma by colorimetry. Lactic acid measurements that evaluate the acid-base status are used in the diagnosis and treatment of lactic acidosis (abnormally high acidity of the blood).

Codes / lots: All Lots

Reason for recall

N-Acetylcysteine (NAC) present in the blood of patients treated for paracetamol overdose can interfere with the Trinder reaction that uses hydrogen peroxide catalytic on aminoantipyrine and phenol, and can produce falsely low results with the reagents using the Trinder reaction method.

FDA-determined cause: Under Investigation by firm

Action taken

Customer notification letters were sent on 01/11/16. Customers were provided the following instructions/actions: When performing tests that use the Tinder reaction, the blood draw should be done before treatment is given to the patient. Reagent inserts for the concerned HORIBA Medical Products have been updated and now include the following additional warning: Patients treated with N-Acetylcysteine (NAC) for Paracetamol overdose may generate a false low result. The letter request customers share the information with laboratory staff and retain the notification as part of their laboratory documentation. The letter states it is mandatory for customers to complete and return the enclosed response form within 10 days in order for the firm to verify the understanding of the notice. If any questions contact the local HORIBA Medical representative.

Details

Recall number
Z-0741-2016
Initiated
January 11, 2016
Posted by FDA
February 2, 2016
Terminated
June 7, 2016
Product code
KHP – Acid, Lactic, Enzymatic Method
Quantity
216
Distribution
U.S. distribution to the following; CA, NY, AL, OK, MN, MS, MD, TX, KY, WV, MT, IL, FL, VA, WA, MI, KS, NE, PA, OH, ID, OR, AR, AZ, NM, NC, SC, GA, TN No foreign distribution.
Recalling firm
Horiba Instruments Inc, Irvine, CA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0738-2016 Class IIThe ABX PENTRA Cholesterol CP ref. A11A01634 is an in vitro diagnostic assay for…N-Acetylcysteine (NAC) present in the blood of patients treated for paracetamol overdose can interfere with… 01/11/2016Terminated
Z-0739-2016 Class IIABX PENTRA Enzymatic Creatinine CP ref. A11A01907 reagent is intended for the…N-Acetylcysteine (NAC) present in the blood of patients treated for paracetamol overdose can interfere with… 01/11/2016Terminated
Z-0740-2016 Class IIABX PENTRA Glucose PAP CP ref. A11A01668 reagent is intended for the quantitative in…N-Acetylcysteine (NAC) present in the blood of patients treated for paracetamol overdose can interfere with… 01/11/2016Terminated
Z-0742-2016 Class IIABX PENTRA Triglycerides CP ref. A11A01640 is an in vitro diagnostic assay for the…N-Acetylcysteine (NAC) present in the blood of patients treated for paracetamol overdose can interfere with… 01/11/2016Terminated
Z-0743-2016 Class IIABX PENTRA Uric Acid CP ref. A11A01670 is an in vitro diagnostic assay for the…N-Acetylcysteine (NAC) present in the blood of patients treated for paracetamol overdose can interfere with… 01/11/2016Terminated