- Recalling firm
- Siemens Medical Solutions USA, Inc
- Reason for recall
- Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
- Affected products (lot / model / serial)
- Model Number: 11327700. UDI-DI: 4056869149325. Serial Numbers: 174132, 174128, 174085, 174152, 174056, 174055, 174083, 174121, 174122, 174087, 174044, 174061, 174099, 174058, 174063, 174150, 174126, 174125, 174096, 174145, 174101, 174065, 174076, 174078, 174091, 174149, 174059, 174073, 174081, 174067.
- Units affected
- 30 units
- Distribution pattern
- US Nationwide distribution.
- Firm location
- Malvern, PA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2643-2026
- Recall initiated
- May 20, 2026
- FDA classification date
- July 1, 2026
- FDA report date
- July 8, 2026
- FDA event ID
- 99079
- Last updated on HTM Vibe
- July 23, 2026