Device recall: Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7, HEMO-10, HEMO-7-EU, HEMO-10-EU Software Version: N/A Product Description: Hemostatic device for endoscopic gastrointestinal use Component: No
Official structured record identifier: 99452.
Publisher
USA
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- Publisher
- openFDA Device Recalls
- Region
- USA
- Scope
- Regulatory
- Published
- September 23, 2026
- Language
- EN
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Official structured record identifier: 99452.
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Source: openFDA Device Recalls
Scope: Regulatory
Evidence: Tier 1 路 Regulatory source
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