# FDA recall Z-1436-2026

> **MRIMed Inc.** · Class II · device recall initiated 2025-10-13.

## 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 for recall

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

## Distribution

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.

## Key facts

- **Recall number:** Z-1436-2026
- **Recalling firm:** MRIMed Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-13
- **Report date:** 2026-03-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Petaluma, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1436-2026

## Citation

> AI Analytics. FDA recall Z-1436-2026. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-1436-2026. Source: US FDA. Licensed CC0.

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