Bokser Home 100% Cotton Mattress Pads
Anhui Zhongqinghonyu Home Textile Technology Co. LTD, of China
Summary
CPSC recall: Bokser Home 100% Cotton Mattress Pads. By Anhui Zhongqinghonyu Home Textile Technology Co. LTD, of China. Hazard: The recalled mattress pads violate the mandatory federal flammability regulation for mattress pads, posing a fire hazard.. Remedy: Consumers should stop using the recalled mattress pads immediately and contact Bokser Home for a full refund. Consumers who purchased the mattress pads will be asked to destroy the product by cutting it with scissors and sending Bokser Home a
Details
Source
CPSC Consumer Product Recall
External ID
9825
Action Date
2024-01-18
Status
Recalled
Category
consumer_product
Product Description
This recall involves all sizes of Bokser Home 100% cotton mattress pads manufactured after October 2022. The quilted box
Context & Analysis
This is a unclassified recall.
This was one of 7 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Anhui Zhongqinghonyu Home Textile Technology Co. LTD, of China 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 (Anhui Zhongqinghonyu Home Textile Technology Co. LTD, of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Anhui Zhongqinghonyu Home Textile Technology Co. LTD, of China have FDA actions?
Anhui Zhongqinghonyu Home Textile Technology Co. LTD, of China 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 "9825" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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