LeMaitre Vascular, Inc.: Medical Device Recalls in 2019

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by LeMaitre Vascular, Inc. in 2019. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

The LeMaitre Aortic Occlusion Catheter is a single lumen catheter with a latex balloon, it is offered in two balloon sizes: 28 mm or 45mm. The single lumen acts as the inflation lumen for the balloon and is indicated by the white stopcock. Other features include a balloon wall thickness designed to reduce the possibility of puncture by calcium deposits, and a stop-cock to maintain balloon inflation level throughout the procedure.