FDA Device recall Z-3064-2017
Tissu-Trans Filtron 2000, 3-TT-FILTRON 2000
- FDA Device
- Class II
- terminated
- Published 2017-08-30
On 2017-08-30 the FDA classified a Class II recall of Tissu-Trans Filtron 2000, 3-TT-FILTRON 2000 by Shippert Medical Technologies, citing seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3064-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-01 |
| Published | 2017-08-30 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Shippert Medical Technologies |
| Distribution | US |
Product
Tissu-Trans Filtron 2000, 3-TT-FILTRON 2000. Product Usage: Intended for fat transfer and liposuction.
Reason
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Identifiers
| code_info | Lot Numbers 11947, 12003, 12078, 12110. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3064-2017%22
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