LeMaitre Vascular, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1444-2017)

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 Reddick Cholangiogram Catheter with introducer(eIFU) REF # e2400-52

Product Classification:

Class II

Date Initiated: February 7, 2017

Date Posted: March 22, 2017

Recall Number: Z-1444-2017

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: 608

Code Information:

Lot Number/Ex Date: RED1746 2018-09 RED1753 2018-12 RED1762 2019-03 RED1765 2019-03 RED1779 2019-09

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