Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc. Due to Extremely low absorbance readings.
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 Alfa Wassermann, Inc. directly.
Affected Products
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.
Quantity: SA1047 lot F3609: 146; RX1047 lot F3610: 53
Why Was This Recalled?
Extremely low absorbance readings.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Alfa Wassermann, Inc.
Alfa Wassermann, Inc. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report