Date Initiated by Firm | October 06, 2017 |
Create Date | February 04, 2018 |
Recall Status1 |
Terminated 3 on July 02, 2019 |
Recall Number | Z-0521-2018 |
Recall Event ID |
78863 |
510(K)Number | K160743 |
Product Classification |
System, x-ray, tomography, computed - Product Code JAK
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Product | Philips Ingenuity CT computed tomography x-ray system |
Code Information |
Ingenuity Core 128 - 728323 SN# - 4001 4016 9056 9067 9071 9074 9099 9112 9134 9194 9213 9235 9251 9263 9268 9269 9272 9280 9367 9515 9515 9521 9529 9538 9541 9548 9549 9554 9559 9561 9573 9574 9579 9584 9600 9607 9614 9618 9625 9631 9633 9638 9640 9646 9649 9653 9656 9659 9667 9670 9678 9686 9688 9689 9703 9707 9711 9720 9738 9740 9755 9761 9763 9781 9782 9788 9802 9805 9808 9811 9822 9833 9837 9838 9859 9862 9864 9867 9876 9890 9898 9901 9909 9910 9917 9920 9922 9923 9927 9930 9933 9950 9969 9983 9989 9993 9996 9997 10012 10014 10021 10024 10032 10042 10046 10047 10050 10051 10060 10069 10072 10076 10077 10092 10099 10102 10106 10121 10137 10150 10151 10173 10179 10180 10193 10200 10203 10206 10206 10207 10208 10213 10216 10221 10247 10250 10255 10288 10299 10302 10307 10310 10316 10351 10379 10391 10394 10418 10422 10446 10470 10473 10474 10503 10514 10519 10540 10561 10566 10574 10580 10599 10605 10610 10659 10671 10698 10708 10733 10743 10773 29002 29005 29014 29025 29034 29049 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Recalling Firm/ Manufacturer |
Philips Medical Systems (Cleveland) Inc 595 Miner Rd Cleveland OH 44143-2131
|
For Additional Information Contact | Holly Wiight Lee 440-483-5777 |
Manufacturer Reason for Recall | Numerous issues related to software Brilliance iCT 4.1.6 software version.
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FDA Determined Cause 2 | Software design |
Action | Philips Medical Systems (Cleveland), Inc. sent the Customer Information Letter via certified letters mail with returned receipts. Also, a Field Service Engineer will perform the software update on the system to resolve the issues. Implementation of the software update will be monitored. |
Distribution | 26 US Govt accounts |
Total Product Life Cycle | TPLC Device Report |
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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.
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510(K) Database | 510(K)s with Product Code = JAK
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