Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination Recalled by Instrumentation Laboratory Due to Labeled On-board instrument stability issue for current and...
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 Instrumentation Laboratory directly.
Affected Products
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACLTOP¿ Family, ACL TOP Family 50 Seriest and ACL Elite¿/Elite Pro) Part Number: 0020302601
Quantity: 40,224
Why Was This Recalled?
Labeled On-board instrument stability issue for current and future lots, reduced On-board Instrument Stability from 7 days to 5 days
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Instrumentation Laboratory
Instrumentation Laboratory has 38 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report