PuraSinus Absorbable Nasal Hemostat — Class II medical device recall Z-0744-2022
Terminated recall by 3-D Matrix, Inc., reported 2022-03-16, distributed nationwide. The boxes used by the shipper were not validated for use during transport.
| Recall number | Z-0744-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | 3-D Matrix, Inc., Newton, MA, United States |
| Recall initiated | 2019-12-02 |
| Classified | 2022-03-10 |
| Reported by FDA | 2022-03-16 |
| Terminated | 2023-08-25 |
| Distributed | Nationwide (US) |
| Quantity | 3 units |
| UPC / GTIN / UDI-DI | 00860001820829 |
| Lot numbers | 19E30A50 |
| Model numbers | 651-006 |
Product
PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006
Reason for recall
The boxes used by the shipper were not validated for use during transport.
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-0744-2022. 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.