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[Recalled] LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53 — The Contains Latex symbol was not printed onto the box label or the sterile (in… | FDA 2017-02-07

recall fda device united-states

Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.

Recall details

ProductLeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53
Brand / manufacturerLeMaitre Vascular, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1445-2017
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date07 February 2017

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch

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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