SIEMENS Biograph mCT: a) Flow 64-4R Seismic, b) S(40)-3R Seismic, c) S(64)-3R Seismic, d) S(40)-4R Seismic, e) S(64)-4R Seismic, f) S(20)-3R Mobile
Reported: February 22, 2023 Initiated: January 16, 2023 #Z-1135-2023
Product Description
SIEMENS Biograph mCT: a) Flow 64-4R Seismic, b) S(40)-3R Seismic, c) S(64)-3R Seismic, d) S(40)-4R Seismic, e) S(64)-4R Seismic, f) S(20)-3R Mobile
Reason for Recall
This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc.
- Units Affected
- 6 units
- Distribution
- Worldwide distribution - US Nationwide and the countries of Japan, Chile, Australia.
- Location
- Hoffman Estates, IL
Frequently Asked Questions
What product was recalled? ▼
SIEMENS Biograph mCT: a) Flow 64-4R Seismic, b) S(40)-3R Seismic, c) S(64)-3R Seismic, d) S(40)-4R Seismic, e) S(64)-4R Seismic, f) S(20)-3R Mobile. Recalled by Siemens Medical Solutions USA, Inc.. Units affected: 6 units.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 22, 2023. Severity: Moderate. Recall number: Z-1135-2023.
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