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U.S. Department of Health and Human Services

Class 2 Device Recall SmartTarget

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 Class 2 Device Recall SmartTargetsee related information
Date Initiated by FirmDecember 23, 2025
Date PostedFebruary 03, 2026
Recall Status1 Open3, Classified
Recall NumberZ-1243-2026
Recall Event ID 98137
510(K)NumberK170250 
Product Classification System, image processing, radiological - Product Code LLZ
ProductFocalyx Fusion
Code Information UDI-DI: 00860003552001. Software Versions: 1.3, 1.5, 1.6. Serial Numbers: IF-FF-B-1-22080504, IF-FF-B-1-TPAA998118, IF-FF-B-1-351238, IF-FF-B-1-TPAB081335, IF-FF-B-1-22080508, IF-FF-B-1-TPAB200331, IF-FF-B-1-TPAB200333, IF-FF-B-1-TPAC505383, IF-FF-B-1-TPAB200348, IF-FF-B-1-TPAB540364, IF-FF-B-1-S5ARQL009253NYZ, IF-FF-B-1-SCARQL0014096YZ, IF-FF-B-1-TPAB532163, IF-FF-B-1-SCARQL00136033KK, IF-FF-B-1-TPAB540359, IF-FF-B-1-TPAB081326, IF-FF-B-1-22080505, IF-FF-B-1-TPAB081324
Recalling Firm/
Manufacturer		 Focalyx Technologies, LLC.
2140 W 68th St Ste 204
Hialeah FL 33016-1815
For Additional Information ContactAlesandra Pluchino
888-636-2259
Manufacturer Reason
for Recall		Software device that is an accessory for image-guided interventional and diagnostic procedures involving prostate has accessories that may not function properly with Windows 10, which may cause patient harm during biopsy or cause treatment/therapy delays, so firm is recommending stop use until device is verified/validated with Windows 11.
FDA Determined
Cause 2		Software change control
ActionOn 12/23/2025, correction notices started being emailed to customers informing them of the following: You will be contacted to schedule installation of the new version. An IFU will be provided at time of installation. Complete and return the response form via email to corporate@focalyx.com If there are any questions, contact the firm at: focalyxtechnologies.com/contact, support@focalyxtechnologies.com, (888) 636 2259, (Sel. 3 Technical Support)
Quantity in Commerce18
DistributionWorldwide - US Nationwide distribution in the states of NY, MA, FL and the countries of ES, VE, DO.
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database510(K)s with Product Code = LLZ
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