Narskido Infant Bath Seats
Yiwu Jingtong Maternal and Infant Products Co. Ltd., of China
Summary
CPSC recall: Narskido Infant Bath Seats. By Yiwu Jingtong Maternal and Infant Products Co. Ltd., of China. Hazard: The bath seats fail to meet the federal safety standard for infant bath seats, including requirements for stability and leg openings, and can tip over while in use, posing a drowning hazard to babies.. Remedy: Consumers should immediately stop using the recalled infant bath seats and contact TopGlore through the Amazon platform for a full refund of the purchase price. Consumers will
Details
Source
CPSC Consumer Product Recall
External ID
9643
Action Date
2023-06-08
Status
Recalled
Category
consumer_product
Product Description
This recall involves Narskido infant bath seats. The molded plastic bath seats are light blue and white and have suction
Context & Analysis
This is a unclassified recall.
This was one of 13 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Yiwu Jingtong Maternal and Infant Products 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 (Yiwu Jingtong Maternal and Infant Products 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 Yiwu Jingtong Maternal and Infant Products Co. Ltd., of China have FDA actions?
Yiwu Jingtong Maternal and Infant Products 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 "9643" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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