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VIBRAPOST
B& L Biotech, inc. · Model VPE · UDI-DI 08800019110293
10
510(k) clearances
100
Adverse events
2
Recalls
126
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-12-05 | Young Dental Manufacturing I, LLC | mislabeled product |
| 2018-07-02 | Water Pik, Inc. | Charging base may overheat with localized melting and sparking, possibly causing fire, shock or burns. |
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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.
