Data Foundry

Medical device recalls 2017

Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000 — Class II medical device recall Z-0170-2018

Terminated recall by Shippert Medical Technologies, reported 2017-11-29. Potential breach of sterility of the packaging.

Recall numberZ-0170-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmShippert Medical Technologies, Centennial, CO, United States
Recall initiated2017-10-20
Classified2017-11-22
Reported by FDA2017-11-29
Terminated2018-10-09
Countries outside the USAU, NL
Quantity56 units
Reason classessterility
Lot numbers12004
Model numbers1000, 3-TT-FILTRON

Product

Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000. Used for fat transfer and liposuction.

Reason for recall

Potential breach of sterility of the packaging.

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-0170-2018. 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.