Smith & Nephew Medical RENASYS EDGE The RENASYS EDGE pump is indicated for patients who recall — FDA Z-0516-2025
Due to issues with battery depletion and inability to recharge if the batteries are not appropriately maintained.
Overview of recall records associated with Smith & Nephew Medical, Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Due to issues with battery depletion and inability to recharge if the batteries are not appropriately maintained.
This page summarizes recall records in which the official source identifies Smith & Nephew Medical, Ltd. 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.