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Duckworth & Kent
DUCKWORTH AND KENT LIMITED · Model 33-202 · UDI-DI 05055313806387
2
510(k) clearances
11
Adverse events
2
Recalls
80
Facilities
Description
Needle Holder
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-11-20 | Becton Dickinson and Company | No Fluid Flow or Restricted Fluid Flow: Nucleus Hydrodissector(s) were found to have reduced or no fluid flow. |
| 2007-11-20 | Becton Dickinson and Company | No Fluid Flow or Restricted Fluid Flow: Nucleus Hydrodissector(s) were found to have reduced or no fluid flow |
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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.