Mederi Stretta Catheter and Accessory Kit, Sterile For Use with the MEDERI MDRF1 GENERATOR recall — FDA Z-2050-2017
Product sterility compromised due to breach in sterile barrier package
Overview of recall records associated with Mederi Therapeutics, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Product sterility compromised due to breach in sterile barrier package
This page summarizes recall records in which the official source identifies Mederi Therapeutics, Inc. 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.