M2R Pro and Warrior Mini Flashlights
Summary
CPSC recall: M2R Pro and Warrior Mini Flashlights. By Olightstore.com, Amazon.com and through small independent stores nationwide from November 2019 through November 2021 for between $48 and $120.. Hazard: The flashlights can be turned on inadvertently and overheat while stored in the holster or a consumer's pocket, posing a burn hazard to consumers.. Remedy: Consumers should immediately stop using the recalled flashlights and contact Olight for a full refund in the form of a store credit or for
Details
Source
CPSC Consumer Product Recall
External ID
9256
Action Date
2022-03-09
Status
Recalled
Category
consumer_product
Product Description
This recall involves M2R Pro and Warrior Mini flashlights. The M2R Pro was sold in black, camouflage, desert tan, OD gre
Context & Analysis
This is a unclassified recall.
This was one of 8 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Olightstore.com, Amazon.com and through small independent stores nationwide from November 2019 through November 2021 for between $48 and $120.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Olightstore.com, Amazon.com and through small independent stores nationwide from November 2019 through November 2021 for between $48 and $120. have FDA actions?
This is the only FDA action we have on record for Olightstore.com, Amazon.com and through small independent stores nationwide from November 2019 through November 2021 for between $48 and $120. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9256" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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