Reported Jun 1, 2016 · Terminated

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

Accriva Diagnostics Inc., dba ITC, dba Accumetrics

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Accriva Diagnostics Inc., dba ITC, dba Accumetrics · 6260 Sequence Dr · San Diego, CA · 92121-4358

Is this the product you have?

  • Accriva- APTT Cuvette for use on the Hemochron Jr. test system, catalog #J103, lot B6JCA012.
Lot codes and dates
  • Lot #B6JCA012
Amount recalled
135 boxes

Where it was sold

Why it was 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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 14, 2016 · Data as of Sep 19, 6:03 PM UTC

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