# FDA recall Z-3064-2017

> **Shippert Medical Technologies** · Class II · device recall initiated 2017-06-01.

## Product

Tissu-Trans Filtron 2000, 3-TT-FILTRON 2000.    Product Usage:  Intended for fat transfer and liposuction.

## Reason for recall

Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

## Distribution

Worldwide Distribution - US Nationwide in the states of:  AL, AR, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, KY, MD, MI, MN, MO, NC, NJ, NV, NY, OH, OR, PA, TN, TX, UT, VA, WA, WV.  and the countries of: Italy, Austria, Turkey, United Arab Emirates, Germany, Spain, Saudi Arabia, Switzerland, Japan Kuwait, Denmark, Sweden, United Kingdom, Belgium, France, Australia, Netherlands, Greece, South Korea.

## Key facts

- **Recall number:** Z-3064-2017
- **Recalling firm:** Shippert Medical Technologies
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-01
- **Report date:** 2017-08-30
- **Termination date:** 2024-01-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Centennial, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3064-2017

## Citation

> AI Analytics. FDA recall Z-3064-2017. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-3064-2017. Source: US FDA. Licensed CC0.

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