Date Initiated by Firm | June 27, 2018 |
Date Posted | August 17, 2018 |
Recall Status1 |
Terminated 3 on April 30, 2024 |
Recall Number | Z-2868-2018 |
Recall Event ID |
80577 |
510(K)Number | K090625 |
Product Classification |
Solid state x-ray imager (flat panel/digital imager) - Product Code MQB
|
Product | EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050 |
Code Information |
Serial Numbers:
SN17000027
SN16000011
SN16000014
SN16000036
SN16000015
SN15000050
476034/SN12000027
476338/SN12000026
SN17000022
SN15000029
SN16000017
SN16000009
SN13000078
SN16000048
SN16000004
SN13000029
SN14000068
511923/SN12000044
514827/SN12000098
514827/SN12000098
SN14000044
***Updated 5/6/21***
SN15000055 |
Recalling Firm/ Manufacturer |
Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany
|
For Additional Information Contact | Philips Service Engineer 40-50782110 |
Manufacturer Reason for Recall | The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient. |
FDA Determined Cause 2 | Device Design |
Action | On June 27, 2018, Philips Medical Systems issued URGENT FIELD SAFETY NOTICES, Medical Device Recall letters to customers. Customers were encouraged to always check the right position of the hook and ensure that the hook is locked according tot he IFU. Press hook down until it is locked. Make sure that the hook is in position. A Philips Service Engineer will contact impacted customers as soon as the Field Action Kit is ready to be implemented. Should you need to communicate with Philips in regards to this program, please reference FCO-71200185. If you need further information or support concerning this issue, please contact your local Philips representative. |
Distribution | US Nationwide; International to 66 countries |
Total Product Life Cycle | TPLC 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.
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510(K) Database | 510(K)s with Product Code = MQB
|