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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

MRIMed MRI LED Mobile Exam Light Battery Recalled for Overheating Risk

Agency Publication Date: February 20, 2026
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Summary

MRIMed Inc. is recalling 314 units of the MRI LED Mobile Exam Light Battery (Model SL-111). The recall was initiated because the battery component can overheat while charging, which may melt internal components and cause smoke. These batteries are used in clinical settings with the SL-110 Mobile Exam Light and were distributed worldwide, including 37 U.S. states and the District of Columbia.

Risk

The battery can overheat during its charging cycle, leading to the melting of internal parts and the release of smoke, which poses a fire and respiratory hazard in a medical environment.

What You Should Do

  1. Immediately stop using the recalled MRI LED Mobile Exam Light Battery (REF SL-111).
  2. Check the serial number on the battery label to see if your unit is affected. See the Affected Products section below for the full list of affected codes.
  3. Contact the manufacturer, MRIMed Inc., or your distributor to arrange for a return, replacement, or correction of the device.
  4. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: MRI LED Mobile Exam Light Battery REF SL-111
Variants: Non-magnetic
Model / REF:
SL-111
Serial Numbers (254):
23-12-074
23-12-039
0
2006001
2006002
2006004
2006005
2006006
2006007
2006008
2006009
2006011
2006012
2006013
2006014
2006015
2006016
2006017
2006018
2006020
2006021
2006023
2006024
2006026
2006027
2006028
2006029
2006030
2006031
2006032
2006033
2006034
2006035
2006038
2006039
2006040
2006043
2204028
2204047
2206001
2206003
2206004
2206005
2206006
2206009
2206010
2206011
2206012
2206013
2206014
UDI:
Pending Information

Quantity: 314 batteries. Serial number 2006025 confirmed and switched in records with Everett Clinic (row 312). Serial 2006026 confirmed for Prince William Med Ctr.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98127
Status: Active
Manufacturer: MRIMed Inc.
Sold By: Medical distributors; MRIMed Inc.
Manufactured In: United States
Units Affected: 314 batteries
Distributed To: Alabama, California, Pennsylvania, South Carolina, Georgia, Massachusetts, Texas, Ohio, New York, North Carolina, Iowa, Washington, Tennessee, New Jersey, Missouri, Louisiana, Minnesota, Arizona, Virginia, Kentucky, Florida, Maryland, Indiana, Alaska, Wisconsin, New Mexico, District of Columbia, Rhode Island, Connecticut, Colorado, Oklahoma, Delaware, Nebraska, Illinois, New Hampshire

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.