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ERGOPLANT
Aesculap AG · Model DX811R · UDI-DI 04038653452002
LYS
Prescription
4
510(k) clearances
1,273
Adverse events
1
Recalls
85
Facilities
Description
ERGOPLANT BONE-MILL-CLEANER COARSE 197MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-10-20 | Medtronic Sofamor Danek USA Inc | Metal bone fragmentor was causing metal shavings to be released into the resultant fragmented tissue during use. |
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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.