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AESCULAP
AESCULAP, INC. · Model MB986R · UDI-DI 04046964589737
GDR
Prescription
2
510(k) clearances
5
Adverse events
1
Recalls
84
Facilities
Description
GIGLI SAW HANDLE LOOP STYLE PR
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-05-11 | Argon Medical Devices, Inc | Argon Medical has received a complaint from one of their distributors of a potential packaging defect. The product is sealed in a pouch and the defect if present shows as a potent |
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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.