Recall company profile

CareFusion 203, Inc. Recalls

Overview of recall records associated with CareFusion 203, Inc., including dates, categories and classifications where available.

1recall records
Oct 1, 2014latest record date
Oct 1, 2014earliest record date

Recall history in this database

Classification mix: Class I: 1.

Medical DeviceOct 1, 2014

CareFusion EnVe and ReVel Ventilators recall — FDA Z-2593-2014

CareFusion has identified a potential for damage to the power connector on the EnVe and ReVel ventilators due to misconnection by the operator. The input port on the ventilators must have…

Class IFDA: TerminatedCareFusion 203, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies CareFusion 203, 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.