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Epredia
SHANDON DIAGNOSTICS LIMITED · Model HM325 ROTARY MICROTOME E · UDI-DI 05051663005128
5
510(k) clearances
56
Adverse events
1
Recalls
27
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-08-12 | Richard-Allan Scientific Company | The firm has received two complaints of finger lacerations in operators of this device. |
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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.