# FDA recall Z-1333-2019

> **Shippert Medical Technologies** · Class II · device recall initiated 2018-02-02.

## Product

Tissu-Trans FILTRON 1000, Catalog 3-TT-FILTRON 1000, sterile, disposable, one-patient use.  The firm name on the label is Shippert Medical Technologies, Centennial, CO.

## Reason for recall

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## Distribution

Distribution was nationwide, including PR.   There was government/military distribution.    Foreign distribution was made to Australia, Austria, Belgium, Denmark, Germany, Greece, India, Italy, Japan, Netherlands, New Zealand, Saudi Arabia, South Africa, Spain, Sweden, Switzerland, and United Kingdom,

## Key facts

- **Recall number:** Z-1333-2019
- **Recalling firm:** Shippert Medical Technologies
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2018-02-02
- **Report date:** 2019-05-22

- **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-1333-2019

## Citation

> AI Analytics. FDA recall Z-1333-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1333-2019. Source: US FDA. Licensed CC0.

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