Recall StatusOpen, Classified
Date Initiated2018-02-21
Product Quantity18
Reason for Recall
With certain software versions, import of enhanced ultrasound formatted data/ultrasound images into 3D viewer, (for digital image processing/review/analysis/communication/media interchange acquired from CT/MRI/ultrasound, and pre-operative analysis of surgical options), can result in incorrect display of image orientation, which could result in misdiagnosis or incorrect surgical treatment plan.
Firm Action
On 2/21/2018, correction notices were emailed to customers who were asked to do the following:
a) Affected software versions should not be used with Enhanced 3D Ultrasound DICOM compliant volumes or Philips 3DDCM.
b) If clinicians are utilizing Enhanced 3D Ultrasound DICOM compliant volumes or Philips 3DDCM volume data sets, verify, retrospectively, any potential risk to health to patients and further determine if patients need to be reevaluated and report this information to the firm.
c) Pass a copy of this notice to those staff members who need to be aware of the issue and maintain awareness for a three-month period.
d)If devices were transferred to other departments or organizations, provide a copy of this notice to these consignees.
Firm will contact customers to provide information about the timing and delivery mechanisms of the software upgrade.
If you have questions, contact the firm at: 1-844-273-7766 x2
Distribution Pattern
Worldwide - US Nationwide distribution in the states of CA, OH, NJ, PA, MA, FL, CT, TX, LA, MI, MN and the country of CA.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.