Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Accriva- APTT Cuvette for use on the Hemochron Jr. test system Recalled by Accriva Diagnostics Inc., dba ITC, dba Accumetrics Due to Clot activating reagent mis-positioned or visibly absent in...
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 Accriva Diagnostics Inc., dba ITC, dba Accumetrics directly.
Affected Products
Accriva- APTT Cuvette for use on the Hemochron Jr. test system, catalog #J103, lot B6JCA012.
Quantity: 135 boxes
Why Was This Recalled?
Clot activating reagent mis-positioned or visibly absent in the cuvette's test channel causing APTT test to either have an error code or an erroneously high result.
Where Was This Sold?
This product was distributed to 1 state: VA
About Accriva Diagnostics Inc., dba ITC, dba Accumetrics
Accriva Diagnostics Inc., dba ITC, dba Accumetrics has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report