FDA Device recall Z-2541-2019
Hemospray Endoscopic Hemostat
- FDA Device
- Class II
- terminated
- Published 2019-09-25
On 2019-09-25 the FDA classified a Class II recall of Hemospray Endoscopic Hemostat by Wilson Cook Medical, citing potential for Hemospray device to be unable to spray powder due to misassembly of devices.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2541-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-24 |
| Published | 2019-09-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Wilson Cook Medical |
| Distribution | US |
Product
Hemospray Endoscopic Hemostat
Reason
Potential for Hemospray device to be unable to spray powder due to misassembly of devices.
Identifiers
| code_info | Model Numbers: HEMO-10, HEMO-10-EU, HEMO-7-EU; Lot Codes: W4179646, W4180858, W4180861, W4181073, W4180860, W4181071, W4189223, W4189224 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2541-2019%22
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