Vascular Solutions, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0113-2021)

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.

Product Classification:

Class I

Date Initiated: August 31, 2020

Date Posted: October 28, 2020

Recall Number: Z-0113-2021

Event ID: 86433

Reason for Recall:

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

Status: Terminated

Product Quantity: 2990 units

Code Information:

Model Number: 5550, UDI 10841156100537 total 2990, Lots: 637973, 640204, 659555, 660597, 633668, 663767, 669593, 659856, 644096, 676528, 672481, 632704, 656792, 658273, 666755, 635885.

Distribution Pattern:

Domestic Distribution: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL ,GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ,NM ,NV ,NY ,OH ,OK,OR, PA ,PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY. International Distribution: Austria, Australia, Belgium, Bulgaria, Canada, Cyprus, Czech Republic, France, Germany, Greece, Hong Kong, Ireland, Israel, Italy, Mexico, Netherlands, Oman, Poland, Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, United Arab Emirates and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated