FDA recall, , Moderate risk
MRIMed MRI LED Mobile Exam Light Battery
Due to battery component overheating while charging resulting in melting of internal components and causing smoke.
Summary by Recall Canary from the FDA notice
What happened
MRIMed Inc. of Petaluma, California, recalled 314 MRI LED Mobile Exam Light Battery REF SL-111 batteries because battery component overheating while charging resulted in melting of internal components and caused smoke. The battery is used with the SL-110 Mobile Exam Light. The recall began October 13, 2025, and was added to the FDA's Enforcement Report on February 20, 2026.
The batteries were distributed nationwide 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 and Canada.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your battery affected?
Affected if its lot code is listed.
MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery
- Lot code
- 23-12-074
- 23-12-039
- 2006001
- 2006002
- 2006004
- 2006005
- 2006006
- 2006007
- 2006008
- 2006009
- 2006011
- 2006012
- 2006013
- 2006014
- 2006015
- 2006016
- 2006017
- 2006018
- 2006020
- 2006021
- 2006023
- 2006024
- 2006026
- 2006027
- 2006028
- 2006029
- 2006030
- 2006031
- 2006032
- 2006033
- 2006034
- 2006035
- 2006038
- 2006039
- 2006040
- 2006043
- 2204028
- 2204047
- 2206001
- 2206003
- 2206004
- 2206005
- 2206006
- 2206009
- 2206010
- 2206011
- 2206012
- 2206013
- 2206014
- 2206015
- 2206016
- 2206017
- 2206018
- 2206019
- 2206020
- 2206021
- 2206022
- 2206024
- 2206026
- 2206027
- 2206029
- 2206030
- 2206033
- 2206034
- 2206036
- 2206037
- 2206038
- 2206040
- 2206042
- 2206043
- 2206044
- 2206045
- 2206046
- 2206048
- 2206049
- 2206050
- 2206052
- 2206053
- 2206054
- 2206055
- 2206056
- 2206057
- 2206058
- 2206059
- 2206060
- 2206062
- 2206063
- 2206064
- 2206065
- 2206066
- 2206067
- 2206068
- 2206069
- 2206070
- 2206071
- 2206072
- 2206073
- 2206074
- 2206075
- 2206076
- 2206077
- 2206079
- 2206080
- 2206081
- 2206082
- 2206083
- 2206084
- 2206085
- 2206086
- 2206087
- 2206088
- 2206090
- 2206092
- 2206093
- 2206094
- 2206095
- 2206096
- 2206097
- 2206098
- 2206099
- 2206100
- 2301228
- 2311040
- 2311058
- 2312001
- 2312002
- 2312003
- 2312004
- 2312005
- 2312006
- 2312007
- 2312008
- 2312009
- 2312010
- 2312011
- 2312012
- 2312013
- 2312014
- 2312015
- 2312016
- 2312018
- 2312019
- 2312020
- 2312021
- 2312022
- 2312023
- 2312024
- 2312025
- 2312026
- 2312027
- 2312029
- 2312030
- 2312031
- 2312033
- 2312034
- 2312035
- 2312036
- 2312037
- 2312038
- 2312039
- 2312041
- 2312042
- 2312044
- 2312045
- 2312047
- 2312049
- 2312050
- 2312051
- 2312052
- 2312053
- 2312054
- 2312055
- 2312056
- 2312057
- 2312058
- 2312059
- 2312060
- 2312061
- 2312062
- 2312064
- 2312065
- 2312066
- 2312067
- 2312068
- 2312070
- 2312071
- 2312072
- 2312074
- 2312075
- 2312076
- 2312077
- 2312078
- 2312079
- 2312080
- 2312081
- 2312082
- 2312083
- 2312084
- 2312087
- 2312089
- 2312090
- 2504001
- 2504003
- 2504004
- 2504005
- 2504006
- 2504007
- 2504008
- 2504010
- 2504011
- 2504013
- 2504014
- 2504015
- 2504016
- 2504017
- 2504018
- 2504021
- 2504022
- 2504025
- 2504026
- 2504029
- 2504030
- 2504031
- 2504032
- 2504035
- 2504036
- 2504038
- 2504039
- 2504040
- 2504044
- 2504047
- 2504049
- 2504050
- 2504051
- 2504054
- 2504055
- 2504056
- 2504058
- 2504059
- 2504068
- 2504072
- 2504073
- 2504075
Recall details
- Company began the recall
- Sold in
Worldwide - U.S. Nationwide distribution in the states of Alabama, California, Pennsylvania, South Carolina, Georgia, Massachusetts, Texas, Ohio, New York, North Carolina, Iowa, Washington, Tennessee, New Jersey, Missouri, Louisiana, Minnesota, Arizona, Virginia, South Carolina, Kentucky, Florida, Maryland, Indiana, Alaska, Wisconsin, New Mexico, District of Columbia, Rhode Island, Connecticut, Colorado, Oklahoma, Delaware, Nebraska, Maryland, Illinois, New Hampshire and the countries of Germany, Canada.
- Company
- MRIMed Inc.Petaluma, California
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98127
- Recall number
- Z-1436-2026
- Quantity recalled
- 314 batteries
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
