LeMaitre Vascular, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1452-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU) REF# e2401-53

Product Classification:

Class II

Date Initiated: February 7, 2017

Date Posted: March 22, 2017

Recall Number: Z-1452-2017

Event ID: 76476

Reason for Recall:

The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch

Status: Terminated

Product Quantity: 2065

Code Information:

Lot Number/Exp. Date: RST2392 2018-09 RST2400 2018-10 RST2408 2018-12 RST2419 2019-04 RST2431 2019-04 RST2436 2019-05 RST2447 2019-08

Distribution Pattern:

Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK

Voluntary or Mandated:

Voluntary: Firm initiated