BUTTERFLY iQ/iQ+ WIRELESS CHARGER KIT WTD1A05Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00866646000268), received between Oct 13, 2020 and Oct 13, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Electrical Shorting” (1 report).

2 other recalls cover devices cleared under the same FDA submission (K163510); they may or may not involve this specific model.

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 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 13, 2020Thermal Decomposition of Device; Electrical Shorting; No Apparent Adverse Event; Thermal Decomposition of Device; Electrical Shorting; No Apparent Adverse Event

  THIS IS A FOLLOW UP 2/FINAL REPORT TO PROVIDE A CONCLUSION TO THE INVESTIGATION. REFERENCE INITIAL REPORT FOR EVENT DESCRIPTION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10674288 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K163510. One submission often covers many models, so check the product and lot details in each record.

• Z-1600-2020 · Feb 24, 2020 · Terminated
  Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder Volume Tool is a segmentation measurement tool REF/Model: 850-20003 Software versions 1.13.0, 1.14.0, and
• Z-1601-2020 · Feb 24, 2020 · Terminated
  Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction) Tool REF/Model: 850-20003 UDI: (01)00866646000206 Software versions 1.10.0, 1.11.0, 1.12.0, 1.13.0, 1.13.0,