FDA recall record

SIEMENS Biograph Vision: a) 450, b) 600, c) 600 Edge recall — FDA Z-1136-2023

This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.

Class IIclassification
Z-1136-2023official record ID
Feb 22, 2023report date

Recall record at a glance

Official recordZ-1136-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmSiemens Medical Solutions USA, Inc.
Report dateFeb 22, 2023
Recall initiation dateJan 16, 2023
Quantity4 units
LocationHoffman Estates, IL, United States

Official product description

SIEMENS Biograph Vision: a) 450, b) 600, c) 600 Edge

Why the product was recalled

This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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