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RecallWatchMedical Device Safety
Class IIOngoingZ-1436-2026

MRIMed Inc. recalls MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved ba…

MRIMed Inc.Petaluma, CA, United StatesReported Mar 4, 2026 · 4 months ago
Legal News Analyst ·

Reason for recall

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

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • 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
    UDI-DI codeModel Number
    266 affected lots
    23-12-07423-12-039200600120060022006004200600520060062006007
    +258 more2006008200600920060112006012200601320060142006015200601620060172006018200602020060212006023200602420060262006027200602820060292006030200603120060312006032200603320060342006035200603820060392006040200604322040282204047220600122060032206004220600522060062206009220601022060112206012220601322060142206015220601622060172206018220601922060202206021220602222060242206026220602722060292206030220603322060342206036220603722060382206040220604222060432206044220604522060462206048220604922060502206052220605322060542206055220605622060572206058220605922060602206062220606322060642206065220606622060672206068220606922060702206071220607222060732206074220607522060762206077220607922060802206081220608222060832206084220608522060862206087220608822060902206092220609322060942206095220609622060972206098220609922061002301228231104023110582312001231200223120032312004231200523120062312007231200823120092312010231201123120122312013231201423120152312016231201823120192312020231202123120222312023231202423120252312026231202723120292312030231203123120332312034231203523120362312036231203723120382312039231204123120412312042231204423120452312047231204923120502312051231205223120532312054231205523120562312057231205823120592312060231206123120622312064231206523120662312067231206823120702312071231207223120742312075231207623120772312078231207923120802312080231208123120822312082231208323120842312087231208923120902504001250400325040042504005250400625040072504008250401025040112504013250401425040152504016250401725040182504021250402225040252504026250402925040302504031250403225040352504036250403825040392504040250404425040472504049250405025040512504054250405525040562504058250405925040682504072250407325040752006025312044200602620060263112006xxx2006xxx2006xxx2006xxx2006xxx2006xxx2006xxx2006xxx2006xxx2006xxx2006xxx2206025

What the firm is doing

On or about 10/13/2025, the firm called customers and emailed an "URGENT MEDICAL DEVICE QUARANTINE" Letter to customer and distributers informing them that the firm has become aware of the possibility of the battery overheating during charging, resulting in melting of the internal components. Customers and Distributors are instructed to: 1. Immediately discontinue use of the battery. 2. Do not charge the battery. 3. Remove the charger from the battery. 4. Label the battery and the light as BATTERY IN QUARANTINE, DO NOT USE 5. Keep the batteries in a secure location to avoid unintended use, and await further instructions from MRI Med. For Distributors are instructed to cease distribution of the affected products. For Questions - contact MRI Med, Inc. Monday through Friday, 8:00am-3:00pm, PST, or email sales@MRImed.com or via phone at 707-762-8600

DistributionShow details

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.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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