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Hydrodebrider™
MEDTRONIC XOMED, INC. · Model 1913001 · UDI-DI 00763000435905
KMA
Prescription
5
510(k) clearances
24
Adverse events
1
Recalls
96
Facilities
Description
CONSOLE 1913001 HYDRODEBRIDER
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-04-03 | Water Pik, Inc. | Customer complaints related to cross contamination of sinus rinse solution between the battery compartment and solution reservoir used for rinsing nasal passages. |
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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.