Tissu-Trans Filtron 1000 — Class II medical device recall Z-3063-2017
Terminated recall by Shippert Medical Technologies, reported 2017-08-30, distributed nationwide. Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
| Recall number | Z-3063-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Shippert Medical Technologies, Centennial, CO, United States |
| Recall initiated | 2017-06-01 |
| Classified | 2017-08-22 |
| Reported by FDA | 2017-08-30 |
| Terminated | 2024-01-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, CH, DE, DK, ES, FR, GB, GR, IT, JP, KR, KW, NL, SA, SE, TR |
| Quantity | 5,188 units |
| Reason classes | sterility, packaging |
| Lot numbers | 12047, 12077, 61235 |
Product
Tissu-Trans Filtron 1000, 3-TT-FILTRON 1000. Product Usage: Intended for fat transfer and liposuction.
Reason for recall
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3063-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.