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Vascular Solutions, Inc. recalls Langston Dual Lumen Catheter.
Recalled October 28, 2020 · FDA recall Z-0111-2021 · Vascular Solutions
Hazard
The inner lumen of the Langston catheter may separate from the hub during pressure injection. · FDA Class I
Units
89,121 units
Sold at
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.
Description
The inner lumen of the Langston catheter may separate from the hub during pressure injection.
Product
Langston Dual Lumen Catheter.
Manufacturer(s)
Vascular Solutions, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →