Advanced Medical Solutions MEDLINE MAXORB EXTRA ALGINATE WOUND DRESSING 4X4 SQUARE REF recall — FDA Z-0619-2025
Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.
Overview of recall records associated with Advanced Medical Solutions Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 3.
Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.
Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.
Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.
This page summarizes recall records in which the official source identifies Advanced Medical Solutions 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.