Up&Up 3R1Recalls & reported problems
Target Corporation · PWTB POLARIS II BLK SO 2PK · Class 1
Data updated Oct 13, 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 00071031846523), received between Nov 17, 2020 and Nov 17, 2020 — classified as 1 malfunction.
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
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.
MalfunctionNov 17, 2020Material Fragmentation
CONSUMER STATED: I PURCHASED THE (B)(4) INSTEAD OF (B)(4) TOOTHBRUSH FOR THE FIRST TIME AND WAS HIGHLY DISAPPOINTED. AFTER USING THE BRUSH FOR 3 DAYS THE PLASTIC PIECES IN BETWEEN THE BRISTLES STARTED TO BREAK OFF, WHILE I WAS BRUSHING MY TEETH. NO CONSUMER CONTACT INFO PROVIDED, PRODUCT NOT RETURNED.
Patient problems: Insufficient Information
MAUDE report 10856538 ↗
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- Solimo SMPAmazon.Com Services LLC · Toothbrush, Powered2 reports
- CVS Health SMPWoonsocket Prescription Center, Incorporated · Toothbrush, Powered2 reports
- Meijer SMPMeijer, Inc. · Toothbrush, Powered1 report
- OralKleen V1Oralkleen, LLC · Toothbrush, Powered1 report
- Waterpik Sensonic Toothbrush STW-03W020Water Pik, Inc. · Toothbrush, Powered1 report
- CVS Health ULSWoonsocket Prescription Center, Incorporated · 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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