Children's Pajama Sets
Last Word Apparel LTD dba Selfie Craft Company, of United Kingdom
Summary
CPSC recall: Children's Pajama Sets. By Last Word Apparel LTD dba Selfie Craft Company, of United Kingdom. Hazard: The children's pajama sets fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries to children.. Remedy: Consumers should immediately take the recalled pajama sets away from children, stop using them and contact the Selfie Craft Company. Consumers are to destroy the recalled pajama sets by cutting them in half vertically and submitting a photo of
Details
Source
CPSC Consumer Product Recall
External ID
9504
Action Date
2023-01-19
Status
Recalled
Category
consumer_product
Product Description
This recall involves Selfie Craft Company children's pajamas. The pajama sets are a two-piece long-sleeve shirt and pant
Context & Analysis
This is a unclassified recall.
This was one of 17 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Last Word Apparel LTD dba Selfie Craft Company, of United Kingdom 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 (Last Word Apparel LTD dba Selfie Craft Company, of United Kingdom) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Last Word Apparel LTD dba Selfie Craft Company, of United Kingdom have FDA actions?
Last Word Apparel LTD dba Selfie Craft Company, of United Kingdom 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 "9504" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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