3M™ Peltor™ X4 Series Earmuffs
Summary
CPSC recall: 3M™ Peltor™ X4 Series Earmuffs. By 3M Company, of Saint Paul, Minnesota. Hazard: The recalled noise-reducing earmuffs can develop cracks in the colored portion of the plastic cups, posing a risk of overexposure to loud noise and sound.. Remedy: Consumers should immediately stop using the recalled earmuffs and contact 3M to receive free replacement earmuffs, including free shipping..
Details
Source
CPSC Consumer Product Recall
External ID
9929
Action Date
2024-04-25
Status
Recalled
Category
consumer_product
Product Description
This recall involves 3M's Peltor X4 series earmuffs designed for noise reduction in industrial and occupational applicat
Context & Analysis
This is a unclassified recall.
This was one of 10 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
3M Company, of Saint Paul, Minnesota has 2 FDA actions in our database, including 1 recall.
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 (3M Company, of Saint Paul, Minnesota) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does 3M Company, of Saint Paul, Minnesota have FDA actions?
3M Company, of Saint Paul, Minnesota has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9929" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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