Medical DeviceApr 29, 2015
Thermedx Fluid Management System P4000 recall — FDA Z-1463-2015
To correct software bugs that could affect the ability to accurately measure fluid deficit.
Class IIFDA: TerminatedThermedx LLC
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Thermedx LLC 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.