RecallRadar

FDA Device recall Z-2663-2025

MAGNETOM Spectra as the following: 1. MAGNETOM Spectra

On 2025-10-08 the FDA classified a Class I recall of MAGNETOM Spectra as the following: 1. MAGNETOM Spectra by Siemens Medical Solutions Usa, citing 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 desi….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2663-2025
ClassificationClass I
Statusongoing
Initiated2025-08-28
Published2025-10-08
Last updated2026-09-13 11:57 UTC
CompanySiemens Medical Solutions Usa
DistributionUS

Product

MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. MAGNETOM Spectra (CN). Model Number: 10655588.

Reason

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.

Identifiers

code_info
1. Model Number: 10837643. UDI Number: (01)04056869006802(21)72030. Serial Number: 72030. Additional serial number add…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.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2663-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.