Siemens recalls specific models of Biograph Horizon PET/CT scanners due to improper design specifications. Affected units have serial numbers listed in the recall notice. Consumers should contact Siemens for details.
Improper design or specifications.
Siemens is recalling certain models of Biograph Horizon PET/CT scanners because of improper design specifications. This could affect the safety of the equipment used in medical imaging. Affected units have specific serial numbers listed in the recall notice.
The recall states there is an issue with the improper design or specifications of the scanners. However, the specific hazard mechanism is not clearly described in the notice. Without more details on how the design flaw could cause harm, it's unclear what risks exist.
Medical facilities that own or use the recalled Siemens Biograph Horizon PET/CT scanners are most at risk. Patients using these scanners for medical imaging may be affected if the equipment is not properly maintained.
Check if your scanner has a Material Number of 10532746 or 10532748 and the listed serial numbers in the recall notice. The affected units are specific models of Siemens Biograph Horizon PET/CT scanners used for medical imaging.
Reach out to Siemens Medical Solutions USA, Inc. to confirm if your scanner is affected and get instructions on next steps.
The recall states there is an issue with improper design or specifications, but the exact hazard mechanism is not clearly described in the notice.
Check if your scanner has a Material Number of 10532746 or 10532748 and the listed serial numbers in the recall notice.
The recall does not specify a need to stop using the scanner immediately; contact Siemens for details.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-0707-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-0707-2019 from Siemens. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
