Tissu-Trans FILTRON 2000 — Class II medical device recall Z-1334-2019
Completed recall by Shippert Medical Technologies, reported 2019-05-22, distributed nationwide.
| Recall number | Z-1334-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Shippert Medical Technologies, Centennial, CO, United States |
| Recall initiated | 2018-02-02 |
| Classified | 2019-05-15 |
| Reported by FDA | 2019-05-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CH, DE, DK, ES, GB, GR, IN, IT, JP, NL, NZ, SA, SE, ZA |
| Quantity | 6,553 units |
| Model numbers | 2000, 3-TT-FILTRON |
Product
Tissu-Trans FILTRON 2000, Catalog 3-TT-FILTRON 2000, sterile, disposable, one-patient use. The firm name on the label is Shippert Medical Technologies, Centennial, CO.
Reason for recall
Not stated by FDA.
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-1334-2019. 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.