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Solimo SJLRecalls & reported problems

Amazon.Com Services LLC · Flosser, Hi-Tech, Center Pick, Mint · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00842379146930), received between Aug 24, 2020 and May 21, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Fragmentation” (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

  • Material Fragmentation1
  • Product Quality Problem1
  • Use of Device Problem1

Patient problems

  • Failure of Implant1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionMay 21, 2021Product Quality Problem; Use of Device Problem

    REVIEW POSTED ON (B)(6): THEY ARE HORRIBLE LITTLE PICKS. ACTUALLY PULLED MY CROWN OUT. NO CONTACT INFORMATION.

    Patient problems: Failure of Implant

    MAUDE report 11866925 ↗
  • MalfunctionAug 24, 2020Material Fragmentation

    CONSUMER POSTED REVIEW ON AMAZON THAT "THE PLASTIC TOOTHPICK END ALWAYS BREAKS AND THE FLOSS STRING BREAKS AS WELL. UNUSABLE" NO CONTACT INFO PROVIDED

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10446235 ↗

Other Floss, Dental devices

All Floss, Dental devices →

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