Accumetrics Inc. Recalls

Overview of recall records associated with Accumetrics Inc., including dates, categories and classifications where available.

2recall records

Mar 19, 2014latest record date

Dec 18, 2013earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceMar 19, 2014

Accumetrics VerifyNow IIb/IIIa Test, Catalog No. 85310, 10-Test Kit and Catalog No. 85011 recall — FDA Z-1172-2014

Accumetrics is recalling the VerifyNow IIb/IIIa test because it may result in the reporting of an erroneous low platelet aggregation unit (PAU) result. An erroneous low PAU result may cause…

Class IIFDA: TerminatedAccumetrics Inc.

Medical DeviceDec 18, 2013

Accumetrics VerifyNow IIb/IIIa Test, 10-Test Kit, Catalog No. 85310, 10 tests/box recall — FDA Z-0482-2014

Accumetrics is recalling the VerifyNow IIb/IIIa 10-Test because it contains incorrect information for the amount of time in which to perform the test following collection of the patient…

Class IIFDA: TerminatedAccumetrics Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Accumetrics Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.