FDA Device recall Z-1334-2019
Tissu-Trans FILTRON 2000, Catalog 3-TT-FILTRON 2000, sterile, disposable, one-patient use
- FDA Device
- Class II
- completed
- Published 2019-05-22
On 2019-05-22 the FDA classified a Class II recall of Tissu-Trans FILTRON 2000, Catalog 3-TT-FILTRON 2000, sterile, disposable, one-patient use by Shippert Medical Technologies.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1334-2019 |
| Classification | Class II |
| Status | completed |
| Initiated | 2018-02-02 |
| Published | 2019-05-22 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Shippert Medical Technologies |
| Distribution | US |
Product
Tissu-Trans FILTRON 2000, Catalog 3-TT-FILTRON 2000, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Reason
Identifiers
| code_info | 61688, 61759, 61846, 61847, and 61848 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1334-2019%22
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