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Molnlycke Health Care, Inc recalls Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'
Recalled May 24, 2017 · FDA recall Z-2110-2017 · Molnlycke Health Care
Hazard
Sterilization validation failure. · FDA Class II
Units
956 units
Sold at
Domestic: U.S. Nationwide; Foreign: Austria, Australia, Bangladesh, Canada, Chile, Germany, Denmark, Finland, France, Great Britain, Hong Kong, Hungary, Ireland, India, Italy, Jordan, Korea, Kuwait, Malaysia, Norway, New Zealand, Peru, Saudi Arabia, Sweden Switzerland, Taiwan, Turkey, South Africa, United Arab Emirates.
Description
Sterilization validation failure.
Product
Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'
Manufacturer(s)
Molnlycke Health Care, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →