FDA Device recall Z-3066-2017
Tissu-Trans SFILL 360, 3-TT-SFILL 360
- FDA Device
- Class II
- terminated
- Published 2017-08-30
On 2017-08-30 the FDA classified a Class II recall of Tissu-Trans SFILL 360, 3-TT-SFILL 360 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-3066-2017 |
| 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 SFILL 360, 3-TT-SFILL 360. 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 12079, 61117, 61143, 61405. |
|---|
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-3066-2017%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.