Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra Flowable Wound recall — FDA Z-1338-2019
Stability did not meet acceptance criteria for visual appearance during mixing and force vs. displacement at 6 months
Overview of recall records associated with Integra Limited, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Stability did not meet acceptance criteria for visual appearance during mixing and force vs. displacement at 6 months
This page summarizes recall records in which the official source identifies Integra Limited 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.