Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported March 5, 2025
SIGNA MR355, SIGNA MR360, NMRI system
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 …
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Ge Healthcare (China) Co., Ltd. recalled SIGNA MR355, SIGNA MR360, NMRI system - a moderate-severity action.
SIGNA MR355, SIGNA MR360, NMRI system was recalled by Ge Healthcare (China) Co., Ltd. in March 5, 2025. Reason: For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" …. Check the official notice for the remedy. Verify recall #Z-1242-2025 with the FDA Devices before acting.
The recall
Ge Healthcare (China) Co., Ltd. issued this moderate-severity FDA Devices recall-For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" ….
- Moderate
- severity level
- 241 units
- affected scope
- Class II
- classification
- March 5, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1242-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1242-2025) was formally reported on March 5, 2025, with the manufacturer initiating the action on January 31, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. Ge Healthcare (China) Co., Ltd. is listed as the recalling firm, operating out of Beijing, N/A. Federal records list the affected scope as 241.
The documented reason for this recall is: 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… Distribution data in the federal record shows the product reached: Domestic US distribution nationwide. International distribution worldwide.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
241
Related Recalls
6
3 from same agency
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1242-2025 |
| Date reported | March 5, 2025 |
| Date initiated | January 31, 2025 |
| Recalling firm | Ge Healthcare (China) Co., Ltd. |
| Firm location | Beijing, N/A |
| Affected scope | 241 |
| Distribution | Domestic US distribution nationwide. International distribution worldwide. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-1242-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
SIGNA MR355, SIGNA MR360, NMRI system. Recalled by Ge Healthcare (China) Co., Ltd.. Units affected: 241.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 5, 2025. Severity: Moderate. Recall number: Z-1242-2025.
Where was the recalled product distributed? ▼
Distribution: Domestic US distribution nationwide. International distribution worldwide..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1242-2025) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported March 5, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.