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AESCULAP
AESCULAP, INC. · Model MG624 · UDI-DI 04046955057443
FGM
Prescription
7
510(k) clearances
20
Adverse events (1 deaths)
1
Recalls
104
Facilities
Description
PROBE W/EYE D1.65MM 305MM SILVER
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2004-02-06 | Medtronic Gastroenterology / Urology | The product's rear panel label could smear during use causing the serial number to be unreadible. This has the remote possibility of resulting in patient data from diagnostic test |
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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.