CVS Health ULSRecalls & reported problems
Woonsocket Prescription Center, Incorporated · Power Toothbrush, Polaris, Soft · Class 1
All models of CVS Health (16)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00050428432785), received between Dec 8, 2021 and Dec 8, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Slipped” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Device Slipped1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 8, 2021Device Slipped
CONSUMER PURCHASED A 2 PACK OF CVS HEALTH BRAND TOOTH BRUSHES AND THE BRISTLES WERE FALLING OUT CONSUMER RESPONSE: I THREW AWAY THE BRISTLES THAT IT SHED ¿ AS SOON AS I STARTED TO BRUSH ¿ AFTER I RETURNED HOME.
Patient problems: Insufficient Information
MAUDE report 12961161 ↗
Other Toothbrush, Powered devices
- Equate VKGWal-Mart Stores, Inc. · Toothbrush, Powered14 reports
- CVS Health TMLWoonsocket Prescription Center, Incorporated · Toothbrush, Powered4 reports
- Solimo SMPAmazon.Com Services LLC · Toothbrush, Powered2 reports
- CVS Health SMPWoonsocket Prescription Center, Incorporated · Toothbrush, Powered2 reports
- OralKleen V1Oralkleen, LLC · Toothbrush, Powered1 report
- Meijer SMPMeijer, Inc. · Toothbrush, Powered1 report
- Waterpik Sensonic Toothbrush STW-03W020Water Pik, Inc. · Toothbrush, Powered1 report
- Up&Up 3R1Target Corporation · Toothbrush, Powered1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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