Peters Surgical The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are recall — FDA Z-2676-2014
A potential splitting of the surface treatment of the thread ends on certain sutures has recently been identified.
Overview of recall records associated with Peters Surgical, including dates, categories and classifications where available.
Classification mix: Class II: 2.
A potential splitting of the surface treatment of the thread ends on certain sutures has recently been identified.
A potential splitting of the surface treatment of the thread ends on certain sutures has recently been identified.
This page summarizes recall records in which the official source identifies Peters Surgical 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.