Class II — 3-D Matrix, Inc.
| Recalling firm | 3-D Matrix |
|---|---|
| Registered facility | FUSO PHARMACEUTICAL (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The boxes used by the shipper were not validated for use during transport. |
| Product | PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006 |
| Quantity | 3 units |
| Distribution | US Nationwide distribution in the state OH. |
| Initiated | 2019-12-02 |
| Classified | 2022-03-10 |
| Terminated | 2023-08-25 |
| Recall number | Z-0744-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — 3-D Matrix, Inc. (Z-0744-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/89577/
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