Soma Access Systems AxoTrack I Sterile Procedure Kit 18G, K1001-18XTW recall — FDA Z-0215-2015
There is a possibility the sterile packaging may fail before the expiration date specified on the package.
Overview of recall records associated with Soma Access Systems LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
There is a possibility the sterile packaging may fail before the expiration date specified on the package.
This page summarizes recall records in which the official source identifies Soma Access Systems 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.