Data Foundry

Medical device recalls 2026

MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and… — Class II medical device recall Z-1436-2026

Ongoing recall by MRIMed Inc., reported 2026-03-04, distributed nationwide. Due to battery component overheating while charging resulting in melting of internal components and causing sm

Recall numberZ-1436-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMRIMed Inc., Petaluma, CA, United States
Recall initiated2025-10-13
Classified2026-02-20
Reported by FDA2026-03-04
DistributedNationwide (US)
Countries outside the USCA, DE
Quantity314 batteries
Reason classesdevice malfunction
Lot numbers2006001, 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 and 203 more
Serial numbers2006026
Model numbersL-111, SL-111

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1436-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.