Zimmer Surgical Inc. is recalling approximately 11,940 units of its 3:1 Dermacarrier skin graft carriers because they were manufactured with an incorrect mesh pattern. While the packaging states the product provides a 3:1 expansion ratio, the device actually features a 1.5:1 ridge pattern. This manufacturing error affects 76 boxes in the United States and 521 boxes distributed internationally.
Using a carrier with the wrong expansion ratio can lead to minor tissue damage during the skin grafting process. Additionally, if the surgeon anticipates a larger graft area based on the 3:1 label, they may find the skin does not cover the intended area, requiring an unplanned second graft procedure.
Manufacturer notification and guidance
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
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Sources: FDA iRES · Raw API Response
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