Skip to content

Meijer SMPRecalls & reported problems

Meijer, Inc. · Smilesonic Pro Advanced Power Toothbrush · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00713733815673), received between Nov 20, 2020 and Nov 20, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 20, 2020Detachment of Device or Device Component

    CONSUMER STATED WHEN I WAS USING RANIR PREMIUM ANTIPLAQUE SONICARE TOOTHBRUSH HEAD REPLACEMENT. THE TUFTS CAME OUT. I SWALLOWED A FEW AND SPIT OUT THE BLUE.

    Patient problems: Foreign Body In Patient

    MAUDE report 10877280 ↗

Other Toothbrush, Powered devices

All Toothbrush, Powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.