Solimo SMPRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00842379159190), received between Oct 26, 2020 and Nov 24, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 24, 2020Break; Product Quality Problem

  COMPLAINT CAME IN ON (B)(6), "WORST ELECTRIC TOOTHBRUSH IVE EVER OWNED. THE BRISTLES BROKE OFF AND GOT STUCK IN MY GUMS. VERY POOR QUALITY." NO PRODUCT RETURNED, NO CONTACT INFO PROVIDED.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 10891170 ↗
• MalfunctionOct 26, 2020Material Fragmentation

  CONSUMER POSTED ON (B)(4): "I WAS DISAPPOINTED IN THESE BRUSH HEADS. IT WAS SUPPOSED TO BE ENOUGH FOR TO LAST A WHOLE YEAR. TO USE EACH ONE FOR THREE MONTHS. THE BRISTLES WOULD FALL OFF AND THEY WOULD VIBRATE OFF OF THE UNIT" NO FURTHER INFORMATION PROVIDED.

  Patient problems: Insufficient Information

  MAUDE report 10737669 ↗