GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to recall — FDA Z-1734-2025
Due to a potential open seal in the sterile barrier packaging.
Overview of recall records associated with Galt Medical Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 7.
Due to a potential open seal in the sterile barrier packaging.
Due to a potential open seal in the sterile barrier packaging .
Due to a potential open seal in the sterile barrier packaging .
Due to a potential open seal in the sterile barrier packaging.
Due to a potential open seal in the sterile barrier packaging.
Due to a potential open seal in the sterile barrier packaging.
Due to a potential open seal in the sterile barrier packaging .
This page summarizes recall records in which the official source identifies Galt Medical Corporation 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.