MRIMed MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved recall — FDA Z-1436-2026
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
Overview of recall records associated with MRIMed Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
This page summarizes recall records in which the official source identifies MRIMed Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.