Data Foundry

Medical device recalls 2025

SIGNA MR355 — Class II medical device recall Z-1242-2025

Ongoing recall by GE Healthcare (China) Co., Ltd., reported 2025-03-05, distributed nationwide. For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" i

Recall numberZ-1242-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmGE Healthcare (China) Co., Ltd., Beijing, N/A, China
Recall initiated2025-01-31
Classified2025-02-27
Reported by FDA2025-03-05
DistributedNationwide (US)
Quantity241
UPC / GTIN / UDI-DI00082427020120, 00082427030181, 00082427030228, 00082427070248, 00082427070255, 00082427070279, 00082427070309, 00082427070316, 00082427070330, 00082427100501, 00082427110098, 00082427120332, 00082427130201, 00082427160352, 00082427160369, 00082427160406, 00082427190175, 00082427200188, 00082427200218, 00082427220100, 00082427230161, 00082427290073, 00082427310153, 00082427310160, 00195278361257 and 2 more

Product

SIGNA MR355, SIGNA MR360, NMRI system

Reason for recall

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a scan can result in potential excessive tissue heating, especially if the patient is in contact with a conductive material or has an implant.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1242-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.