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MSI Precision Specialty Instruments
Med Saver, Inc. · Model 232-D42-24 · UDI-DI 00194613028879
KAE
Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
225
Facilities
Description
Greven Ear Forceps, Fine Model, Shaft 82mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
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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.