Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ABX PENTRA Uric Acid CP ref. A11A01670 is an in Recalled by Horiba Instruments Inc Due to N-Acetylcysteine (NAC) present in the blood of patients...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Horiba Instruments Inc directly.
Affected Products
ABX PENTRA Uric Acid CP ref. A11A01670 is an in vitro diagnostic assay for the quantitative determination of uric acid in human serum, plasma and urine based on the enzymatic determination of uric acid using a chromogenic system in the presence of peroxidase and uricase (Trinder method).
Quantity: 216
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 29 states: AL, AZ, AR, CA, FL, GA, ID, IL, KS, KY, MD, MI, MN, MS, MT, NE, NM, NY, NC, OH, OK, OR, PA, SC, TN, TX, VA, WA, WV
About Horiba Instruments Inc
Horiba Instruments Inc has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report