FDA Device recall Z-0744-2022
PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006
- FDA Device
- Class II
- terminated
- Published 2022-03-16
On 2022-03-16 the FDA classified a Class II recall of PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006 by 3 D Matrix, citing the boxes used by the shipper were not validated for use during transport.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0744-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-02 |
| Published | 2022-03-16 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | 3 D Matrix |
| Distribution | US |
Product
PuraSinus Absorbable Nasal Hemostat, Part Numbers 651-006
Reason
The boxes used by the shipper were not validated for use during transport.
Identifiers
| code_info | UDI: (01)00860001820829(17)220430(10)19E30A50; Lot Number 19E30A50 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0744-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.