Recall Z-1436-2026— MRIMed Inc.
Class II · Ongoing
Class II FDA medical device recall by MRIMed Inc., initiated 2025-10-13. FDA's recall record names no specific 510(k) clearance for this event. Product: 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. Reason: Due to battery component overheating while charging resulting in melting of internal components and causing smoke..
- Recalling firm
- MRIMed Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-10-13
- Firm location
- Petaluma, CA, United States
Product description
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
Reason for recall
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
Data sourced from openFDA. This site is unofficial and independent of the FDA.