Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to SOMATOM go.Top (Models #11061640 & 11061648) with software...

Date: September 24, 2019
Company: Siemens Medical Solutions USA, Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Medical Solutions USA, Inc directly.

Affected Products

SOMATOM go.Top, Models 11061640 & 11061648- a Computer tomography x-ray system

Quantity: 14 US

Why Was This Recalled?

SOMATOM go.Top (Models #11061640 & 11061648) with software syngo CT VA20A_SP2 and active Guide&GO license No dose documentation and no Dose Alert for the special mode i- Sequence during interventional procedures

Where Was This Sold?

This product was distributed to 7 states: GA, IN, MS, MO, NJ, OH, PA

Affected (7 states)Not affected

About Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc has 613 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report