LeMaitre Vascular, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1446-2017)

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 Scoop Tip Cholangiogram Catheter (eIFU) REF# e2401-50

Product Classification:

Class II

Date Initiated: February 7, 2017

Date Posted: March 22, 2017

Recall Number: Z-1446-2017

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: 4673

Code Information:

Lot Number/Ex p. Date: RST2390 2018-08 RST2393 2018-09 RST2396 2018-10 RST2397 2018-10 RST2398 2018-10 RST2401 2018-12 RST2402 2018-12 RST2418 2019-02 RST2420 2019-03 RST2423 2019-03 RST2428 2019-04 RST2432 2019-04 RST2433 2019-04 RST2437 2019-06 RST2438 2019-06 RST2441 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