Drug recall

The Symbia Intevo series consists of the Intevo 16, Intevo 6 and Intevo 2. This manual also describes the…

FDA recall event 68932 · Class II · Siemens Medical Solutions USA, Inc.

Key facts

Event ID 68932
Recall numbers Z-2712-2014, Z-2713-2014
Recalling firm Siemens Medical Solutions USA, Inc.
Product type Devices
Products The Symbia Intevo series consists of the Intevo 16, Intevo 6 and Intevo 2. This manual also describes the Symbia Intevo Excel. The Symbia Intevo series integrates state-of-the-art SPECT and high…, The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality spiral CT to provide precise attenuation correction and anatomical mapping. The…
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Siemens Medical Solutions USA, Inc. is performing a field correction because we recently detected a rubber isolator with unfavorable aging properties. The function of the rubber isolator, which is…
Initiation date Jul 28, 2014
Report date Oct 8, 2014
Termination date Dec 23, 2016
City Hoffman Estates
State IL
Country United States
FEI number 1000514697

At a glance

  • 1–9 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA drug and product recalls

FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

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