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
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
Recalling Firm: MRIMed Inc.
Grund für den Rückruf / Gefahr
TranslatedDue to battery component overheating while charging resulting in melting of internal components and causing smoke.
Produktbeschreibung & Identifikation
TranslatedMRI 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
Betroffene Produkte
TranslatedMRI 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
Additional Source Details
| Field | Value |
|---|---|
| City | Petaluma |
| State | CA |
| Event id | 98127 |
| Address 1 | 1320 Stub Rd |
| Address 2 | N/A |
| Code info | Model Number: SL-111 UDI-DI code: Pending Information Serial/Lot Numbers: 23-12-074 23-12-039 0 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 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... [TRUNCATED] |
| Postal code | 94954-1122 |
| Report date | 20260304 |
| Product type | Devices |
| Product quantity | 314 batteries |
| Reason for recall | Due to battery component overheating while charging resulting in melting of internal components and causing smoke. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251013 |
| Initial firm notification | Letter |
| Center classification date | 20260220 |
Consumer Action Protocol: What You Should Do Immediately
Safety StepsInspect the NDC code, batch number, or control number on your medicine bottle or blister packaging to confirm whether your unit is included.
Do not abruptly stop critical prescribed medication without physician advice. Contact your dispensing pharmacist immediately for a safe alternative.
Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.
If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (FDA Devices).
Your Legal Rights as a Consumer
Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.
Frequently Asked Questions About This Recall
FAQ GuideQ1:What should I do immediately if I own or bought MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with...?
Check the lot number and NDC on your prescription label. For essential medications, consult your doctor or dispensing pharmacist immediately before abruptly stopping your dose.
Q2:Can I get a full refund or free repair for this recall?
Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.
Q3:Do I need my original sales receipt to claim a remedy or refund?
In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.
Q4:Where can I verify official information for this safety alert?
This safety alert is aggregated directly from official regulatory agency records (FDA Devices). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.
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Übersicht
- Rückrufendes UnternehmenMRIMed Inc.
- StatusOngoing
- RisikostufeClass II
- DistributionWorldwide - 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.
📢 Warnung teilen
Alert family and friends to keep them safe. Copy this quick alert message:
🚨 SAFETY ALERT: MRIMed Inc. - 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 Check if your household is affected: https://therecallfile.com/de/recalls/mri-led-mobile-exam-light-battery-ref-sl-111-this-non-magnetic-ul-and/FDA-Z-1436-2026
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