Home › Schobell Industrial Ltda › Quinelato
Quinelato
Schobell Industrial Ltda · Model QD.280.00 · UDI-DI 07898506841585
EKC
Prescription
2
510(k) clearances
7
Adverse events
8
Recalls
121
Facilities
Description
Discoide Cleoide Carver
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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.