Drug recall
PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006
FDA recall event 89577 · Class II · 3-D Matrix, Inc.
Key facts
| Event ID | 89577 |
|---|---|
| Recall numbers | Z-0744-2022 |
| Recalling firm | 3-D Matrix, Inc. |
| Product type | Devices |
| Products | PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The boxes used by the shipper were not validated for use during transport. |
| Initiation date | Dec 2, 2019 |
| Report date | Mar 16, 2022 |
| Termination date | Aug 25, 2023 |
| City | Newton |
| State | MA |
| Country | United States |
| FEI number | 3015528146 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: