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Hemodent
PREMIER DENTAL PRODUCTS COMPANY · Model 9007073 · UDI-DI 00348783001105
MVL
Prescription
10
510(k) clearances
25
Adverse events
1
Recalls
43
Facilities
Description
Hemodent® liquid 40cc, Pack of 10
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-05-27 | Inter-Med Llc | Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, |
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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.