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SHARPER IMAGE CHBWON-3Recalls & reported problems

Guangdong Okay Technology CO.,Ltd. · Calming Heat Back Wrap.Input DC 5V, 2A, Power 10W. Calming Heat Back Wrap(3settings). 3 Heat,3 Vibration,3 Lumbar. This device complies with part 15 of FCC rules · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 06936189900715), received between Mar 18, 2026 and Mar 18, 2026 — classified as 2 injuries.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (2 reports).

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 2 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Improper or Incorrect Procedure or Method2
  • Use of Device Problem1

Patient problems

  • Full thickness (Third Degree) Burn1
  • Partial thickness (Second Degree) Burn1

Recent adverse event reports

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

  • InjuryMar 18, 2026Improper or Incorrect Procedure or Method

    ON 20-MAR-2026, ADDITIONAL INFORMATION WAS RECEIVED. THE CONSUMER USED THE PRODUCT ON HER BACK WHILE WORKING FOR HOME. SHE REPORTED THE AUTO SHUT OFF NEVER OCCURRED AFTER APPROXIMATELY 4 HOURS OF USE. SHE EXPERIENCED A 3RD DEGREE BURN WITH A BLISTER. SHE WENT TO AN URGENT CARE AND WAS PRESCRIBED SILVADENE CREAM SINCE THE BLISTER HAD ALREADY POPPED. THE BURN TOOK A COUPLE OF WEEKS TO RESOLVE. NO ADDITIONAL INFORMATION WAS PROVIDED.

    Patient problems: Full thickness (Third Degree) Burn

    MAUDE report 24627118 ↗
  • InjuryMar 18, 2026Use of Device Problem; Improper or Incorrect Procedure or Method

    THIS REPORT WAS RECEIVED ON (B)(6) 2023 WHICH REGARDED A FEMALE CONSUMER (AGE NOT PROVIDED) IN ASSOCIATION WITH THE CALMING HEAT BACK WRAP. ON (B)(6) 2023, THE CONSUMER USED A CALMING HEAT BACK WRAP. WHILE USING THE PRODUCT SHE FELT A BURNING SENSATION ON HER BACK. SHE REMOVED THE HEAT WRAP AND DISCOVERED SHE HAD A QUARTER SIZED BLISTER ON THE RIGHT SIDE OF HER BACK. SHE WAS TRANSPORTED TO THE HOSPITAL. SHE WAS NOTED TO HAVE SECOND DEGREE BURNS. SHE WAS ADMITTED AND DISCHARGED FROM THE HOSPITAL ON THE SAME DAY ON (B)(6) 2023. NO FURTHER INFORMATION WAS PROVIDED.

    Patient problems: Partial thickness (Second Degree) Burn

    MAUDE report 24627097 ↗

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Sources and updates

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