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Unity Erodium
Dio Medical, Corp. · Model 000E015060 · UDI-DI 00850051372249
1
510(k) clearances
1,406
Adverse events (5 deaths)
1
Recalls
154
Facilities
Description
Unity Erodium SIJ Screw Ø 15.0 x 60
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-03 | Orthofix U.S. LLC | Labeling contains claims that are not consistently present. |
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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.