Recall company profile

Siemens Medical Solutions USA, Inc. Recalls

Overview of recall records associated with Siemens Medical Solutions USA, Inc., including dates, categories and classifications where available.

390recall records
Jul 8, 2026latest record date
Mar 7, 2018earliest record date

Recall history in this database

Classification mix: Class II: 373, Class I: 16, Class III: 1.

Medical DeviceJan 22, 2020

Siemens ARTIS pheno, Model # 10849000 recall — FDA Z-0807-2020

The potential exists for system movement to be permanently blocked by an activation of the collision sensor integrated in the cover of the collimator even when no collision has occurred.

Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Siemens Medical Solutions USA, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.