SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for necessary patient rescans.
Reported: June 6, 2018 Initiated: April 20, 2018 #Z-1939-2018
Product Description
SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for necessary patient rescans.
Reason for Recall
There is a potential for a software issue that may cause the need for necessary patient rescans.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 4 units in US
- Distribution
- Worldwide Distribution: US (nationwide) including states of: AR, CA, CT, FL, GA, IL, IN, KS, KY, MO, ND, NY, OH, OK, SD, TN, TX, and VA; and countries of: Algeria, Australia, Austria, Bangladesh, Bolivia, Bosnia Herzog., Brazil, Cambodia, Chile, China, Columbia, Costa Rica, Germany, Greece, India, Indonesia, Italy, Japan, Kenya, Kuwait, Lithuania, Mauritius, Morocco, Nepal, Pakistan, Paraguay, Philippines, Poland, Portugal, Republic Korea, Romania, Senegal, Singapore, Slovakia, South Africa, Spain, Switzerland, Thailand, Turkey, Ukraine, and United Kingdom.
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for necessary patient rescans.. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 4 units in US.
Why was this product recalled? ▼
There is a potential for a software issue that may cause the need for necessary patient rescans.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 6, 2018. Severity: Moderate. Recall number: Z-1939-2018.
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