Recall StatusTerminated
Date Initiated2014-03-08
Date Terminated2016-12-05
Product Quantity5 installed in US
Reason for Recall
The A-plane compensator is made of Teflon which will become fragile due to X-ray exposure passing through it. The thinnest part of the compensator is subject to radiation degradation and as a result has been found to fail prematurely. Failure is indicated by pin or ring artifact in the image
Firm Action
Neusoft planned action:
1. Notification of all dealers and purchasers is to be made within 15
working days of receipt of this letter in the manner specified in 21 CFR
1003.21 and 1003.22. This office and the Food and Drug Administration
(FDA) district office coordinator noted below are to be included in the
notification.
2. Neusoft Medical Systems Co., Ltd will implement actions to monitor the
exposures of the tube and when the exposure number is close to
300,000 seconds, the A-plane compensator will be replaced. The Food
and Drug Administration (FDA) district office coordinator should be
notified when the last A-plane compensator is replaced.
3. The Customer Information Letter has been sent to customers as a
corrective action. The maximum exposure number of 5 US systems is
191830 seconds as of Apr.20, 2015, so the firm will monitor the data
continuously and replace the A-plane compensators before the defined
threshold.
4. Neusoft will replace all compensators that have exceeded the 300,000
seconds free of charge and will replace all compensators that fail during
warranty and the compensators failed less than 300,000 seconds
though out of warranty free of charge.
You may proceed or continue with implementation of the CAP (subject to the conditions noted above) For further questions please call (281) 453-1205
Root Cause
Radiation Control for Health and Safety Act
Distribution Pattern
Worldwide Distribution - US Distribution including Puerto Rico and to the states of : IL, MA, TX and SC., and to the countries of : China, Malaysia, Lebanon, Ecuador, Egypt, United Arab Emirates,Kazashstan, Tunisia, Angola, Brazil, Uzbekistan, Lebanon, Cote D' ivoire, South Africa, Montenegro and Tajikistan.
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.