SIEMENS Biograph mCT: a) Flow 64-4R Seismic, b) S(40)-3R Seismic, c) S(64)-3R Seismic, d) S(40)-4R Seismic, e) S(64)-4R Seismic, f) S(20)-3R Mobile
FDA Recall Z-1135-2023 · Posted 2023-02-13
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Recalling FirmSiemens Medical Solutions USA, Inc.
Recall StatusOpen, Classified
Product CodeKPS
Date Initiated2023-01-16
Product Quantity6 units
Reason for Recall
This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.
Firm Action
SIEMENS Healthineers distributed a Consumer Safety Advisory Notice to its consignees on 01/16/2023 by mail and email. The notice explained the issue and recommended that the following preventive actions be taken until a local Siemens Healthineers service representative has applied the correction:
"Mitigation for Biograph Mobile Installations
Ensure that the PET/CT Gantry offset protocol is performed every time the coach has moved. If the PET/CT gantry offset fails due to the results being out of tolerance, please cease clinical operations on the system and contact your local Siemens Healthineers service representative for further evaluation and guidance on how to proceed. Information on how to acquire the PET/CT Gantry offset protocol is documented in your user documentation.
Mitigation for Biograph Seismic Installations
In the event of a seismic event, contact your local Siemens Healthineers service representative for further evaluation and guidance on how to proceed.
Siemens Healthineers will begin dispatching customer service engineers by the end of February 2023 to inspect and make corrections to the locking mechanism to prevent the occurrence of this issue. The resolution for this issue will be delivered by the following Update Instruction: MI516/22/S.
Please ensure that this notice is placed in the Biograph Operator Manual and disseminated to all operators of the scanner."
"If you have any questions regarding this advisory notice, please contact your local Siemens Healthineers representative at the contact numbers provided below.
America: 1-800-888-7436
Europe, Middle East, and Africa: +49 9131 940 4000
Asia and Australia: +86 (21) 3811 2121"
Root Cause
Process control
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Japan, Chile, Australia.
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.
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