LeMaitre Vascular, Inc. has recalled one unit of its Artegraft Vascular Graft due to a labeling mix-up where the product was placed in the incorrect outer packaging for a different lot. This specific unit was distributed in Illinois. Consumers and healthcare providers should identify the affected device by its serial number 24GG298-022 and expiration date of June 28, 2027.
The labeling mix-up means the outer packaging does not accurately reflect the contents of the product, which could lead to a clinician using an incorrect device or relying on inaccurate lot information during a medical procedure.
Labeling mix-up resulting in the incorrect lot outer packaging of product.
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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