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[Recalled] LeMaitre Single Lumen Embolectomy Catheter 3F, 80 cm, Model 1601-38 and e1601-38. Indicated for the removal of arterial emboli and thrombi. — Manufacturing issue that could cause a pinhole in the formed end of the packagi… | FDA

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductLeMaitre Single Lumen Embolectomy Catheter 3F, 80 cm, Model 1601-38 and e1601-38. Indicated for the removal of arterial emboli and thrombi.
Brand / manufacturerLeMaitre Vascular, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-0386-2016
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date21 October 2015

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Manufacturing issue that could cause a pinhole in the formed end of the packaging, which may lead to compromised sterility.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from LeMaitre Vascular, Inc.

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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