CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 recall — FDA Z-0039-2026
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Overview of recall records associated with CORNEAT VISION, LTD., including dates, categories and classifications where available.
Classification mix: Class II: 3.
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Retroactive; Due to complaints, labeling correction for permanent tissue-integrating surgical matrices to include prevention and management of would dehiscence.
This page summarizes recall records in which the official source identifies CORNEAT VISION, 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.