MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. MAGNETOM Spectra (CN). Model Number: 10655588.
Class I - DangerousWhat Should You Do?
- Check if you have this product: 1. Model Number: 10837643. UDI Number: (01)04056869006802(21)72030. Serial Number: 72030. Additional serial number added 11/14/2025: 72023. 2. Model Number: 10655588. UDI Number: (01)04056869006796(21)56069. Serial Number: 56069.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Siemens Medical Solutions USA, Inc
- Reason for Recall:
- There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed venting paths, leading to a pressure build-up within the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. MAGNETOM Spectra (CN). Model Number: 10655588.
Product Codes/Lot Numbers:
1. Model Number: 10837643. UDI Number: (01)04056869006802(21)72030. Serial Number: 72030. Additional serial number added 11/14/2025: 72023. 2. Model Number: 10655588. UDI Number: (01)04056869006796(21)56069. Serial Number: 56069.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2663-2025
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