SIEMENS Biograph Horizon 3R Mobile; System, Tomography, Computed, Emission — FDA record Z-1134-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 16, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
SIEMENS Biograph Horizon 3R Mobile; System, Tomography, Computed, Emission
Reason
This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.
Classification
Class II
Recalling firm
Siemens Medical Solutions USA, Inc.
Quantity
1 unit
Agency-reported status
Ongoing
Source record identifier
Z-1134-2023

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityUDI/DI 405686901102894792, Material Number 10532746, Serial Number 94792

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Worldwide distribution - US Nationwide and the countries of Japan, Chile, Australia.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Feb 22, 2023
Recall initiation date
Jan 16, 2023
Center classification date
Feb 13, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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