Vascular Solutions, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1747-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Langston Dual Lumen Catheter 6F Model 5540. For delivery of contrast medium in angiographic studies

Product Classification:

Class I

Date Initiated: March 16, 2020

Date Posted: May 6, 2020

Recall Number: Z-1747-2020

Event ID: 85350

Reason for Recall:

The inner lumen of the Langston catheter may separate from the hub during pressure injection.

Status: Terminated

Product Quantity: 30,877 units

Code Information:

Model 5540; UDI 10841156100513; Lots 651278, 651457, 651920, 652097, 652176, 652459, 652628, 652777, 653053, 653319, 653443, 653565, 653776, 653863, 654010, 654190, 654340, 654514, 654657, 654889, 654890, 655128, 655287, 655460, 655465, 655738, 655869, 656191, 656533, 656554, 656727, 656801, 657030, 657243, 657517, 657627, 657680, 657866, 658018, 658151, 658250, 658438, 658541, 658671, 658824, 658984, 659122, 659217, 659362, 659443, 659630, 659855, 660075, 660199, 660288, 660397, 660590, 660717, 660823, 660910, 661139, 661257, 661474, 662824

Distribution Pattern:

Worldwide distribution. US nationwide, Austria, Australia, Belgium, Canada, Czech Republic, France, Germany, Greece, Hong Kong, Ireland, Israel, Italy, Mexico, Netherlands, Slovakia, South Africa, Spain, Sweden, Switzerland, and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated