Overview of recall records associated with Somatex Medical Technologies GMBH, including dates, categories and classifications where available.
Classification mix: Class II: 1.
This recall has been initiated due to the risk of wire splintering after contact with a cautery device during the removal of a lesion. There is a potential risk that wire fragments are not…
This page summarizes recall records in which the official source identifies Somatex Medical Technologies GMBH 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.
