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All product recalls associated with LeMaitre Vascular, Inc..
Total Recalls
15
Past Year
6
Class I (Serious)
0
Most Recent
Sep 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The device was incorrectly packed in the wrong size labeled outer packaging.
The bovine carotid arteries used to produce the impacted grafts from affected lots were sourced using raw material from a supplier that had not been reviewed and approved by the appropriate regulatory authority.
Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.