Vascular Solutions, Inc. Langston Dual Lumen Catheter Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Langston Dual Lumen Catheter
Brand
Vascular Solutions, Inc.
Lot Codes / Batch Numbers
Model Number: 5515, UDI 10841156100506 Lot Numbers: 635806, 640206, 644140, 648701, 654143, 658252, 659635, 661470, 665301, 670376, 654130, 672728, 656020, 638111, 677058.
Products Sold
Model Number: 5515, UDI 10841156100506 Lot Numbers: 635806, 640206, 644140, 648701, 654143, 658252, 659635, 661470, 665301, 670376, 654130, 672728, 656020, 638111, 677058.
Vascular Solutions, Inc. is recalling Langston Dual Lumen Catheter due to The inner lumen of the Langston catheter may separate from the hub during pressure injection.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The inner lumen of the Langston catheter may separate from the hub during pressure injection.
Recommended Action
Per FDA guidance
The firm notified consignees that received affected product on August 26, 2020 via UPS Mail (US), email or mail (OUS). The firms immediate correction is to recall the affected devices for destruction. The notice includes instructions on subrecall for any consignees that further distributed affected product.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY, DC, PR
Page updated: Jan 10, 2026