Medical DeviceMar 27, 2019
Covidien, PLC Covidien Force TriVerse electrosurgical device 10 cord-Intended as recall — FDA Z-1020-2019
Potential for the sterile packaging to be compromised
Class IIFDA: TerminatedCovidien, PLC
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 Covidien, PLC 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.