MRIMed Inc.

FDA Regulatory Profile

MRIMed Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1436-2026, Class II) was initiated on October 13, 2025.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1436-2026Class IIMRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is usedOctober 13, 2025