Overview of recall records associated with Covidien, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 112, Class I: 10.
This voluntary recall is being conducted due to the potential for failure to detect the affected Situate" gauze - RF and Xray detectable products by the Situate" detection console due to a…
The device cartridge disengaged during use due to manufacturing error.
This page summarizes recall records in which the official source identifies Covidien, 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.
