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Percutaneous Nephrostomy Dilator
Well Lead Medical Co.,Ltd · Model U02E011220 · UDI-DI 06936881156724
GCC
Prescription
5
510(k) clearances
75
Adverse events (10 deaths)
5
Recalls
100
Facilities
Description
12Fr x 20cm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-07-31 | DePuy Spine, Inc. | Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared. |
| 2013-07-31 | DePuy Spine, Inc. | Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared. |
| 2013-07-31 | DePuy Spine, Inc. | Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared. |
| 2013-07-31 | DePuy Spine, Inc. | Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared. |
| 2013-07-31 | DePuy Spine, Inc. | Dilators and Holding Clip are being used for a secondary function of neuromonitoring, for which it is not 510(k) cleared. |
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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.