MAGNETOM Vida Fit. Model Number: 11410481.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Model Number: 11410481. UDI Numbers: (01)04056869245188(21)202129, (01)04056869245188(21)202025, (01)04056869245188(21)202139, (01)04056869245188(21)202016, (01)04056869245188(21)202051, (01)04056869245188(21)202055, (01)04056869245188(21)202114, (01)04056869245188(21)202119, (01)04056869245188(21)202013, (01)04056869245188(21)202050, (01)04056869245188(21)202102, (01)04056869245188(21)202160, (01)04056869245188(21)202127, (01)04056869245188(21)202071, (01)04056869245188(21)202078, (01)04056869245188(21)202123, (01)04056869245188(21)202082, (01)04056869245188(21)202107, (01)04056869245188(21)202031, (01)04056869245188(21)202110, (01)04056869245188(21)202108, (01)04056869245188(21)202101, (01)04056869245188(21)202093, (01)04056869245188(21)202104, (01)04056869245188(21)202028, (01)04056869245188(21)202026, (01)04056869245188(21)202076, (01)04056869245188(21)202142, (01)04056869245188(21)202125, (01)04056869245188(21)202155, (01)04056869245188(21)202084, (01)04056869245188(21)202151, (01)04056869245188(21)202068, (01)04056869245188(21)202135, (01)04056869245188(21)202121, (01)04056869245188(21)202006, (01)04056869245188(21)202010, (01)04056869245188(21)202011, (01)04056869245188(21)202146, (01)04056869245188(21)202145. Serial Numbers: 202129, 202025, 202139, 202016, 202051, 202055, 202114, 202119, 202013, 202050, 202102, 202160, 202127, 202071, 202078, 202123, 202082, 202107, 202031, 202110, 202108, 202101, 202093, 202104, 202028, 202026, 202076, 202142, 202125, 202155, 202084, 202151, 202068, 202135, 202121, 202006, 202010, 202011, 202146, 202145.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. 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 Vida Fit. Model Number: 11410481.

Product Codes/Lot Numbers:

Model Number: 11410481. UDI Numbers: (01)04056869245188(21)202129, (01)04056869245188(21)202025, (01)04056869245188(21)202139, (01)04056869245188(21)202016, (01)04056869245188(21)202051, (01)04056869245188(21)202055, (01)04056869245188(21)202114, (01)04056869245188(21)202119, (01)04056869245188(21)202013, (01)04056869245188(21)202050, (01)04056869245188(21)202102, (01)04056869245188(21)202160, (01)04056869245188(21)202127, (01)04056869245188(21)202071, (01)04056869245188(21)202078, (01)04056869245188(21)202123, (01)04056869245188(21)202082, (01)04056869245188(21)202107, (01)04056869245188(21)202031, (01)04056869245188(21)202110, (01)04056869245188(21)202108, (01)04056869245188(21)202101, (01)04056869245188(21)202093, (01)04056869245188(21)202104, (01)04056869245188(21)202028, (01)04056869245188(21)202026, (01)04056869245188(21)202076, (01)04056869245188(21)202142, (01)04056869245188(21)202125, (01)04056869245188(21)202155, (01)04056869245188(21)202084, (01)04056869245188(21)202151, (01)04056869245188(21)202068, (01)04056869245188(21)202135, (01)04056869245188(21)202121, (01)04056869245188(21)202006, (01)04056869245188(21)202010, (01)04056869245188(21)202011, (01)04056869245188(21)202146, (01)04056869245188(21)202145. Serial Numbers: 202129, 202025, 202139, 202016, 202051, 202055, 202114, 202119, 202013, 202050, 202102, 202160, 202127, 202071, 202078, 202123, 202082, 202107, 202031, 202110, 202108, 202101, 202093, 202104, 202028, 202026, 202076, 202142, 202125, 202155, 202084, 202151, 202068, 202135, 202121, 202006, 202010, 202011, 202146, 202145.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2668-2025

Related Recalls

During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing 0, an actual x-ray dose is applied to the patient.

Mar 9, 2026 Other Medical Devices View Details →
Class I - Dangerous

During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing 0, an actual x-ray dose is applied to the patient.

Mar 9, 2026 Other Medical Devices View Details →

ARTIS Pheno VE30A and VE40A, Model 10849000

Siemens Medical Solutions USA

Class I - Dangerous

During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result of a constant unregulated medium dose and the angular change of patient diameter caused by rotational acquisition. This may result in unintentional low-dose radiation exposure to a patient.

Mar 12, 2026 Other Medical Devices View Details →