LeMaitre Vascular, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1442-2017)

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 (eIFU) REF# e2400-50

Product Classification:

Class II

Date Initiated: February 7, 2017

Date Posted: March 22, 2017

Recall Number: Z-1442-2017

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: 5601

Code Information:

Lot Number/Exp. Date: RED1743 2018-09 RED1744 2018-09 RED1749 2018-10 RED1750 2018-12 RED1751 2018-12 RED1755 2018-12 RED1756 2018-12 RED1757 2019-01 RED1759 2019-02 RED1760 2019-02 RED1761 2019-03 RED1764 2019-03 RED1766 2019-04 RED1767 2019-04 RED1768 2019-05 RED1769 2019-05 RED1771 2019-06 RED1773 2019-07 RED1774 2019-07 RED1775 2019-07

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