| | Class 2 Device Recall GE Healthcare Centricity |  |
| Date Initiated by Firm | October 03, 2024 |
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| Date Posted | November 07, 2024 |
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| Recall Status1 |
Open3, Classified |
| Recall Number | Z-0318-2025 |
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| Recall Event ID |
95512 |
| 510(K)Number | K131977 |
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| Product Classification |
System, image processing, radiological - Product Code LLZ
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| Product | GE Healthcare Centricity Universal Viewer Zero Footprint, Model Numbers:
1) 2089507-083, GDZH-JINWAN-Centricity
2) 2089507-093, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02268286, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02030900, 1495-1-Centricity Universal Viewer Zero Footprint / ZFP-02347996, 423834-Centricity Universal Viewer Zero Footprint / ZFP-02286658, 1407636-Centricity Universal Viewer Zero Footprint / ZFP-02304121, 651240-Centricity Universal Viewer Zero Footprint / ZFP-02173181, 268034-Centricity Universal Viewer Zero Footprint / ZFP-02402520;
3) 2089507-098, JP-310027-Centricity Universal Viewer Zero Footprint / ZFP-02033125;
4) 2089507-109, 3909-2-Centricity Universal Viewer Zero Footprint / ZFP-20095312, 3909-2-Centricity Universal Viewer Zero Footprint / ZFP-20095313, 327750-Centricity Universal Viewer Zero Footprint / ZFP-02184508;
5) 2089507-111, 105468-1-Centricity Universal Viewer Zero Footprint / ZFP-02254840, 1495-3-Centricity Universal Viewer Zero Footprint / ZFP-00096090, JP-340111-Centricity Universal Viewer Zero Footprint / ZFP-01275379, JP-275353-Centricity Universal Viewer Zero Footprint / ZFP-02042636;
6) 2089507-112, 3922-25-Centricity Universal Viewer Zero Footprint / ZFP-01290685, 3922-17-Centricity Universal Viewer Zero Footprint / ZFP-00098229, 1503586-Centricity Universal Viewer Zero Footprint / ZFP-21016603, RU0994-Centricity Universal Viewer Zero Footprint / ZFP-02331255;
7) 2089507-114, 1461-1-Centricity Universal Viewer Zero Footprint / ZFP-02360229, 1461-1-Centricity Universal Viewer Zero Footprint / ZFP-01803680, 3728-2-Centricity Universal Viewer Zero Footprint / ZFP-01225897, 3728-2-Centricity Universal Viewer Zero Footprint / ZFP-01225898, 3728-2-Centricity Universal Viewer Zero Footprint / ZFP-01225904, 3728-2-Centricity Universal Viewer Zero Footprint / ZFP-01371500, M51725-Centricity Universal Viewer Zero Footprint / ZFP-01300873, M1781854-Centricity Universal Viewer Zero Footprint / ZFP-01553772, 609334-Centricity Universal Viewer Zero Footprint / ZFP-01282257, UJJF01-Centricity Universal Viewer Zero Footprint / ZFP-22186138, CMC-Centricity Universal Viewer Zero Footprint / ZFP-01820241, JP-100014-Centricity Universal Viewer Zero Footprint / ZFP-01890709, KW1102-Centricity Universal Viewer Zero Footprint / ZFP-02191178, 59219_ERPerror-Centricity Universal Viewer Zero Footprint / ZFP-02327073, QA1114-Centricity Universal Viewer Zero Footprint / ZFP-02306397, SAU1433-Centricity Universal Viewer Zero Footprint / ZFP-01457278, TTSH-CVIS-Centricity Universal Viewer Zero Footprint / ZFP-02041523, NE4651-Centricity Universal Viewer Zero Footprint / ZFP-00038599, NE6703-Centricity Universal Viewer Zero Footprint / ZFP-00038552, NE6731-Centricity Universal Viewer Zero Footprint / ZFP-00038461, NE3006-Centricity Universal Viewer Zero Footprint / ZFP-00038362, NE2196-Centricity Universal Viewer Zero Footprint / ZFP-00038588, NPV738-Centricity Universal Viewer Zero Footprint / ZFP-00038637, NE2031-Centricity Universal Viewer Zero Footprint / ZFP-00038578, NE7405-Centricity Universal Viewer Zero Footprint / ZFP-00038372, NE2162-Centricity Universal Viewer Zero Footprint / ZFP-00038563, NE4878- |
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| Code Information |
UDI/DI 00840682102988 for all models:
1) 2089507-083, Installed Product ID Numbers: GDZH-JINWAN-Centricity Universal Viewer Zero Footprint / ZFP-02171477, 103378-Centricity Universal Viewer Zero Footprint / ZFP-20039058, 1664823-Centricity Universal Viewer Zero Footprint / ZFP-20080654, 493356-Centricity Universal Viewer Zero Footprint / ZFP-20085691, Medireport-Centricity Universal Viewer Zero Footprint / ZFP-02291850, Medireport-Centricity Universal Viewer Zero Footprint / ZFP-02291877, Medireport-Centricity Universal Viewer Zero Footprint / ZFP-02292580, 81077-Centricity Universal Viewer Zero Footprint / ZFP-20680055, IL1469-Centricity Universal Viewer Zero Footprint / ZFP-02156638, JP-110145-Centricity Universal Viewer Zero Footprint / ZFP-01275393, 1333629-Centricity Universal Viewer Zero Footprint / ZFP-01300332;
2) 2089507-093, Installed Product ID Numbers: 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02268286, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02030900, 1495-1-Centricity Universal Viewer Zero Footprint / ZFP-02347996, 423834-Centricity Universal Viewer Zero Footprint / ZFP-02286658, 1407636-Centricity Universal Viewer Zero Footprint / ZFP-02304121, 651240-Centricity Universal Viewer Zero Footprint / ZFP-02173181, 268034-Centricity Universal Viewer Zero Footprint / ZFP-02402520;
3) 2089507-098, Installed Product ID Numbers: JP-310027-Centricity Universal Viewer Zero Footprint / ZFP-02033125;
4) 2089507-109, Installed Product ID Numbers: 3909-2-Centricity Universal Viewer Zero Footprint / ZFP-20095312, 3909-2-Centricity Universal Viewer Zero Footprint / ZFP-20095313, 327750-Centricity Universal Viewer Zero Footprint / ZFP-02184508;
5) 2089507-111, Installed Product ID Numbers:
6) 2089507-112, Installed Product ID Numbers:
7) 2089507-114, Installed Product ID Numbers:
8) 2089507-115, Installed Product ID Numbers:
9) 2089507-116, Installed Product ID Numbers:
10) 2089507-117, Installed Product ID Numbers:
11) 2089507-118, Installed Product ID Numbers:
12) 2089507-119, Installed Product ID Numbers:
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| FEI Number |
3004526608
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Recalling Firm/
Manufacturer |
GE Healthcare
500 W Monroe St
Chicago IL 60661-3671
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| For Additional Information Contact | GE HealthCare Service
800-437-1171 |
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Manufacturer Reason
for Recall | GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) where there is a potential security vulnerability which could allow a malicious actor to access the system and potentially manipulate patient data. |
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FDA Determined
Cause 2 | Software Manufacturing/Software Deployment |
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| Action | GE Healthcare issued an URGENT MEDICAL DEVICE CORRECTION notice to it consignees on 10/03/2024 via letter issued through a traceable means. The notice explained the issue and provided the following actions be to be implemented until the devices can be corrected:
Option 1: Restrict access to these systems from the internet.
or
Option 2: Implement additional safeguards such as a VPN.
For questions or concerns regarding this notification, please contact GE HealthCare Service at 1-800-437-1171 or a local Service Representative.
GE HealthCare will correct all affected products at no cost. A GE HealthCare representative will make contact to arrange for the correction. |
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| Quantity in Commerce | 120 units |
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| Distribution | Worldwide distribution - United States Nationwide and the countries of Algeria, Argentina, Brazil, China, Dominican Republic, France, Germany, India, Indonesia, Ireland, Israel, Japan, Kuwait, Malaysia, Mexico, Panama, Qatar, Russia, Saudi Arabia, Singapore, Spain, United Kingdom. |
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| 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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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| 510(K) Database | 510(K)s with Product Code = LLZ
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