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HEMOBLAST Bellows
DILON TECHNOLOGIES FRANCE · Model BQF02 · UDI-DI 03760193182705
PMX
Prescription
0
510(k) clearances
25
Adverse events
2
Recalls
12
Facilities
Description
Hemostatic agent, including thrombin
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-06 | Baxter Healthcare Corporation | Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the produ |
| 2018-05-30 | Baxter Healthcare Corporation | Baxter r recalled this device due to the use of an incorrect plastic formulation in the manufacture of the blue luer component of the FLOSEAL malleable tips. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.