Molnlycke Health Care EZ Derm Porcine Xenograft, labeled as the following: a recall — FDA Z-1243-2019
Intermittent heat seal failures on the outer pouch of some EZ Derm products.
Overview of recall records associated with Molnlycke Health Care, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Intermittent heat seal failures on the outer pouch of some EZ Derm products.
This page summarizes recall records in which the official source identifies Molnlycke Health Care, 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.