# FDA recall Z-1747-2020

> **Vascular Solutions, Inc.** · Class I · device recall initiated 2020-03-16.

## Product

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

## Reason for recall

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

## Distribution

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.

## Key facts

- **Recall number:** Z-1747-2020
- **Recalling firm:** Vascular Solutions, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-16
- **Report date:** 2020-05-06
- **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-1747-2020

## Citation

> AI Analytics. FDA recall Z-1747-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1747-2020. Source: US FDA. Licensed CC0.

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