Hemospray Endoscopic Hemostat — Class II medical device recall Z-2541-2019
Terminated recall by Wilson-Cook Medical Inc., reported 2019-09-25, distributed nationwide. Potential for Hemospray device to be unable to spray powder due to misassembly of devices.
| Recall number | Z-2541-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wilson-Cook Medical Inc., Winston Salem, NC, United States |
| Recall initiated | 2019-07-24 |
| Classified | 2019-09-13 |
| Reported by FDA | 2019-09-25 |
| Terminated | 2020-06-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, CA, CY, DE, DK, ES, FR, GB, GR, IT, PT |
| Quantity | 160 units |
| Lot numbers | W4179646, W4180858, W4180860, W4180861, W4181071, W4181073, W4189223, W4189224 |
| Model numbers | HEMO-10, HEMO-10-EU, HEMO-7-EU |
Product
Hemospray Endoscopic Hemostat
Reason for recall
Potential for Hemospray device to be unable to spray powder due to misassembly of devices.
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-2541-2019. 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.