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AESCULAP
AESCULAP, INC. · Model MN092R · UDI-DI 04046964575075
HAE
Prescription
10
510(k) clearances
482
Adverse events (1 deaths)
2
Recalls
64
Facilities
Description
CUSHING RONGEUR DWN DEL 1.5X10MM 228MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-10-30 | Folsom Metal Products, Inc. | Units were not intended for commercial distribution and inadvertently distributed. |
| 2023-10-30 | Folsom Metal Products, Inc. | Units were not intended for commercial distribution and inadvertently distributed. |
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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.