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U.S. Department of Health and Human Services

Class 2 Device Recall Monaco RTP System

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 Class 2 Device Recall Monaco RTP Systemsee related information
Date Initiated by FirmDecember 21, 2016
Create DateJanuary 11, 2017
Recall Status1 Terminated 3 on July 16, 2021
Recall NumberZ-1009-2017
Recall Event ID 76028
510(K)NumberK132971 K151233 
Product Classification System,planning,radiation therapy treatment - Product Code MUJ
ProductMonaco RTP System Product Usage: Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Code Information Software Versions 5.00 and higher
Recalling Firm/
Manufacturer		 Elekta, Inc.
400 Perimeter Center Ter NE Ste 50
Atlanta GA 30346-1227
For Additional Information ContactLinda Wetsel
770-300-9725
Manufacturer Reason
for Recall		Incorrect Enhanced Dynamic Wedge (EDW) or Virtual Wedge (VW) Calculations.
FDA Determined
Cause 2		Nonconforming Material/Component
ActionElekta sent an Urgent Important Field Safety Notification letter dated December 2016 to customers. The notice informs users of the specific product and version numbers affected by the issue and any work arounds that can be used to avoid the issue. The notice included a reply form to be returned to Elekta.
Quantity in Commerce279
DistributionWorldwide Distribution - US Nationwide in the state of CA, IN, KY, MA, NJ, NY, NC, PA, TX, WI, and the countries of Brazil, Canada, China, Croatia, Estonia, Germany, India, Japan, Netherlands, New Zealand, Norway, Poland, Serbia, South Africa, Spain, Russia, Turkey
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 = MUJ
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