FDA Device recall Z-2664-2025

MAGNETOM Verio

FDA Device
Class I
ongoing
Published 2025-10-08

On 2025-10-08 the FDA classified a Class I recall of MAGNETOM Verio 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

Agency	FDA Device
Recall number	Z-2664-2025
Classification	Class I
Status	ongoing
Initiated	2025-08-28
Published	2025-10-08
Last updated	2026-09-13 11:57 UTC
Company	Siemens Medical Solutions Usa
Distribution	US

Product

MAGNETOM Verio. Model Number: 10276755.

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	Model Number: 10276755. UDI Numbers: N/A. Serial Numbers: 40649, 40585, 40781, 40243, 40408, 40628, 40848, 40870, 40783… Model Number: 10276755. UDI Numbers: N/A. Serial Numbers: 40649, 40585, 40781, 40243, 40408, 40628, 40848, 40870, 40783, 40473, 40240, 40497, 40564, 40425, 40778, 40389, 40340, 40523, 40582, 40168, 40291, 40283, 40201, 40850, 40331, 40126, 40744, 40821, 40433, 40502, 40179, 40246, 40273, 40766, 40753, 40828, 40737, 40352, 40313, 40382, 40670, 40387, 40631, 40669, 40131, 40541, 40466, 40292, 40375, 40161, 40745, 40268, 40284, 40325, 40799, 40190, 40877, 40104, 40195, 40407, 40640, 40797, 40254, 40142, 40665, 40622, 40264, 40420, 40633, 40150, 40514, 40727, 40710, 40328, 40156, 40800, 40692, 40165, 40441, 40864, 40482, 40472, 40859, 40220, 40858, 40779, 40346, 40295, 40233, 40629, 40681, 40464, 40568, 40200, 40663, 40334, 40277, 40276, 40879, 40222, 40361, 40553, 40378, 40714, 40715, 40252, 40250, 40423, 40204, 40486, 40251, 40488, 40109, 40855, 40429, 40232, 40157, 40440, 40259, 40545, 40556, 40687, 40140, 40237, 40399, 40312, 40235, 40697, 40684, 40398, 40871, 40700, 40368, 40656, 4060

code_info

Model Number: 10276755. UDI Numbers: N/A. Serial Numbers: 40649, 40585, 40781, 40243, 40408, 40628, 40848, 40870, 40783…

Model Number: 10276755. UDI Numbers: N/A. Serial Numbers: 40649, 40585, 40781, 40243, 40408, 40628, 40848, 40870, 40783, 40473, 40240, 40497, 40564, 40425, 40778, 40389, 40340, 40523, 40582, 40168, 40291, 40283, 40201, 40850, 40331, 40126, 40744, 40821, 40433, 40502, 40179, 40246, 40273, 40766, 40753, 40828, 40737, 40352, 40313, 40382, 40670, 40387, 40631, 40669, 40131, 40541, 40466, 40292, 40375, 40161, 40745, 40268, 40284, 40325, 40799, 40190, 40877, 40104, 40195, 40407, 40640, 40797, 40254, 40142, 40665, 40622, 40264, 40420, 40633, 40150, 40514, 40727, 40710, 40328, 40156, 40800, 40692, 40165, 40441, 40864, 40482, 40472, 40859, 40220, 40858, 40779, 40346, 40295, 40233, 40629, 40681, 40464, 40568, 40200, 40663, 40334, 40277, 40276, 40879, 40222, 40361, 40553, 40378, 40714, 40715, 40252, 40250, 40423, 40204, 40486, 40251, 40488, 40109, 40855, 40429, 40232, 40157, 40440, 40259, 40545, 40556, 40687, 40140, 40237, 40399, 40312, 40235, 40697, 40684, 40398, 40871, 40700, 40368, 40656, 4060

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-2664-2025%22

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