# FDA recall Z-0110-2021

> **Vascular Solutions, Inc.** · Class I · device recall initiated 2020-08-31.

## Product

Langston Dual Lumen Catheter

## Reason for recall

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

## Distribution

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.

## Key facts

- **Recall number:** Z-0110-2021
- **Recalling firm:** Vascular Solutions, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-08-31
- **Report date:** 2020-10-28
- **Termination date:** 2024-06-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Maple Grove, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0110-2021

## Citation

> AI Analytics. FDA recall Z-0110-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0110-2021. Source: US FDA. Licensed CC0.

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