MRIMed Inc. Recalls MRI LED Mobile Exam Light Batteries Due to Overheating and Smoke Hazard
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MRIMed Inc. has voluntarily recalled 314 MRI LED Mobile Exam Light batteries (Model SL-111) due to reports of components overheating, melting, and emitting smoke during charging.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 6, 2026 and geographically references Worldwide. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, MedicalDevices.
What Happened
MRIMed Inc. has initiated a voluntary recall of its MRI LED Mobile Exam Light Battery (REF SL-111). The recall was issued following reports that battery components may overheat while charging. This defect can result in the melting of internal components and the emission of smoke, posing a potential safety hazard in medical environments.
Which Products Are Affected
The recall involves 314 units of the MRI LED Mobile Exam Light Battery, Model Number SL-111. These non-magnetic, UL and CE approved batteries are designed for use with the SL-110 Mobile Exam Light.
Affected units include a wide range of serial and lot numbers, including but not limited to:
- 23-12-074, 23-12-039
- Series starting with: 2006, 2204, 2206, 2301, 2311, 2312, and 2504
The products were distributed worldwide, including Germany and Canada. Within the United States, distribution occurred in AL, CA, PA, SC, GA, MA, TX, OH, NY, NC, IA, WA, TN, NJ, MO, LA, MN, AZ, VA, KY, FL, MD, IN, AK, WI, NM, DC, RI, CT, CO, OK, DE, NE, IL, and NH.
What You Should Do
MRIMed Inc. notified affected customers via letter starting in October 2025. Facilities and consumers using these batteries should immediately check their model and serial numbers against the affected list. If you possess a recalled battery, follow the instructions provided in the firm's notification letter regarding the return or replacement of the device. For additional information, contact MRIMed Inc. at their Petaluma, California headquarters.
Why This Matters
Overheating batteries in a clinical or MRI environment present a significant risk of fire and smoke inhalation. Such malfunctions can compromise patient safety and damage sensitive medical equipment during critical examinations.
Source
This information is based on official recall data provided by the U.S. Food and Drug Administration (FDA). Recall Number: Z-1436-2026.
Original source: FDA Official Notice ↗
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