# FDA recall Z-2779-2017

> **Myelotec, Inc.** · Class II · device recall initiated 2017-03-02.

## Product

Myelotec  Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels

## Reason for recall

Obstructed/blocked port from defective VGC Access Port Body component.

## Distribution

Worldwide Distribution - US Distribution to the states of : CA, FL, KY, MN, and NJ ., and to the countries of : Brazil, Iran, Kuwait, Malaysia, Singapore, South Korea, Taiwan, and Turkey

## Key facts

- **Recall number:** Z-2779-2017
- **Recalling firm:** Myelotec, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2017-03-02
- **Report date:** 2017-08-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Roswell, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2779-2017

## Citation

> AI Analytics. FDA recall Z-2779-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2779-2017. Source: US FDA. Licensed CC0.

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