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U.S. Department of Health and Human Services

Class 2 Device Recall Butterfly iQ

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 Class 2 Device Recall Butterfly iQsee related information
Date Initiated by FirmFebruary 24, 2020
Date PostedMarch 17, 2020
Recall Status1 Terminated 3 on June 12, 2020
Recall NumberZ-1600-2020
Recall Event ID 85185
510(K)NumberK163510 
Product Classification System, imaging, pulsed doppler, ultrasonic - Product Code IYN
ProductButterfly 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 1.15.0 - Product Usage: Butterfly iQ is indicated for use by qualified and trained healthcare professionals to enable diagnostic ultrasound imaging and measurement of anatomical structures and fluids of adult and pediatric patients.
Code Information Software versions 1.13.0, 1.14.0, and 1.15.0 UDI: (01)00866646000206
FEI Number 3010102386
Recalling Firm/
Manufacturer		 Butterfly Network, Inc.
530 Old Whitfield St
Guilford CT 06437-3441
Manufacturer Reason
for Recall		Distributed without an approved 510(k)
FDA Determined
Cause 2		No Marketing Application
ActionButterfly Network issued a correction notification via email on February 24, 2020 disabling the Auto Bladder Volume Tool from affected devices operating software versions 1.13.0, 1.14.0 and 1.15.0 for all affected US Butterfly iQ customers and removed references of Auto Bladder Volume Tool from outward marketing platforms. Butterfly Network has notified Affiliate partners to cease marketing the Auto Bladder Volume Tool until further notice. Questions related to this correction can be sent to Butterfly Network Customer Support via email at Support@butterflynetwork.com
Quantity in Commerce15,121 host devices
DistributionUS Nationwide distribution.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 �7.55.
510(K) Database510(K)s with Product Code = IYN
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