Medical device recalls Moderate risk

MRIMed product recalled over fire hazard

Recall date
October 13, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
MRIMed Inc. recalls MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with S…
Recall number
Z-1436-2026
FDA classification
Class II
Brand / firm
MRIMed Inc.
Sold / distributed
Worldwide - U.S. Nationwide distribution in the states of AL, CA, PA, SC, GA, MA, TX, OH, NY, NC, IA, WA, TN, NJ, MO, LA, MN, AZ, VA, SC, KY, FL, MD, IN, AK, WI, NM, DC, RI, CT, CO, OK, DE, NE, MD, IL, NH and the countries of Germany, Canada.

Why it was recalled

Due to battery component overheating while charging resulting in melting of internal components and causing smoke.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with SL-110, Mobile Exam Light

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