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Millennium
Avalign Technologies, Inc. · Model 10-310404 · UDI-DI 00190776086121
DWP
Prescription
10
510(k) clearances
171
Adverse events
1
Recalls
44
Facilities
Description
Garrett Vascular Dilator
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 |
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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.