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AESCULAP
Aesculap AG · Model DC200R · UDI-DI 04038653033898
EKC
Prescription
2
510(k) clearances
7
Adverse events
8
Recalls
121
Facilities
Description
BLACK Excavator, 6 3/4" (170 mm), double ended
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-11-14 | Sybron Dental Specialties | The tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed. |
| 2008-11-14 | Sybron Dental Specialties | The tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed. |
| 2008-11-14 | Sybron Dental Specialties | The tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed. |
| 2008-11-14 | Sybron Dental Specialties | The tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed. |
| 2008-11-14 | Sybron Dental Specialties | The tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed. |
| 2008-11-14 | Sybron Dental Specialties | The tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed. |
| 2008-11-14 | Sybron Dental Specialties | The tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed. |
| 2008-11-14 | Sybron Dental Specialties | The tips of the Neos Vanadium Excavators may prematurely release from the handle during use, and if so, the tip may be accidentally swallowed. |
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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.