Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hemochron Jr. Whole Blood Microcoagulation System APTT Cuvette. For in Recalled by ITC-Nexus Dx Due to Test results may be erroneously elevated or report...
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 ITC-Nexus Dx directly.
Affected Products
Hemochron Jr. Whole Blood Microcoagulation System APTT Cuvette. For in vitro diagnostic coagulation test. Catalog number J103.
Quantity: US- 315 cuvettes; OUS - 2835 cuvettes
Why Was This Recalled?
Test results may be erroneously elevated or report an out-of-range high (OOR-H) error code in non heparinized blood samples.
Where Was This Sold?
Worldwide Distribution - US including the states of Georgia, Virginia and New York., and the countries of Canada, France, Italy, Liechtenstein and Romania.
About ITC-Nexus Dx
ITC-Nexus Dx 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