LeMaitre Vascular, Inc. recalls
5 recalls filed under LeMaitre Vascular, Inc.. The most recent was published October 14, 2026.
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Class II · 11 days ago
LeMaitre Vascular, Inc. TufTex¿ Over-the-Wire Embolectomy Catheter recall: Devices failed in process testing related to the amount of pull force it
Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.
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Class II · 7 months ago
LeMaitre Vascular, Inc. Artegraft Vascular Graft recall: Labeling mix-up resulting in the incorrect lot outer packaging of product
Labeling mix-up resulting in the incorrect lot outer packaging of product.
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Class II · 12 months ago
LeMaitre Vascular, Inc. Artegraft¿ Collagen Vascular Graft recall: The device was incorrectly packed in the wrong size labeled outer packaging
The device was incorrectly packed in the wrong size labeled outer packaging.
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Class II · 1+ years ago
LeMaitre Vascular, Inc. Artegraft Collagen Vascular Graft. Model/Catalog/Part recall: Devices were distributed with incorrect label without CE and UKCA mark
Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.
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Class II · 1+ years ago
LeMaitre Vascular, Inc. Artegraft Collagen Vascular Grafts Model Numbers: AG 616 recall: The bovine carotid arteries used to produce the impacted grafts from affected
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…
About this page
LeMaitre Vascular, Inc. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.