FDAApril 22, 2016device

Accriva- APTT Cuvette for use on the Hemochron Jr. test system, catalog #J103, lot B6JCA012.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

accriva diagnostics inc dba itc dba accumetricsaccrivaaccriva diagnostics

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →