FDA Device recall Z-0170-2018
Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000
- FDA Device
- Class II
- terminated
- Published 2017-11-29
On 2017-11-29 the FDA classified a Class II recall of Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000 by Shippert Medical Technologies, citing potential breach of sterility of the packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0170-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-10-20 |
| Published | 2017-11-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Shippert Medical Technologies |
| Distribution | n/a |
Product
Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000. Used for fat transfer and liposuction.
Reason
Potential breach of sterility of the packaging.
Identifiers
| code_info | Lot 12004 |
|---|
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-0170-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.