Cook Lead Clipper- An auxiliary tool indicated for use in patients requiring percutaneous recall — FDA Z-2513-2023
Sterility of device may be compromised due to breach of the chevron seal of the packaging
Overview of recall records associated with Cook Vandergrift, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Sterility of device may be compromised due to breach of the chevron seal of the packaging
This page summarizes recall records in which the official source identifies Cook Vandergrift, 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.