KICIMPRO Kitchen Faucets, model number KM800-01-06BN
Kaipingshikemuyulinweiyushiyeyouxiangongsi, of China, doing business as Amazon seller Kicimpro
Summary
CPSC recall: KICIMPRO Kitchen Faucets, model number KM800-01-06BN. By Kaipingshikemuyulinweiyushiyeyouxiangongsi, of China, doing business as Amazon seller Kicimpro. Hazard: The recalled faucets were tested and found to contain lead that can leach into water at levels that can be particularly harmful to infants and young children. Lead ingestion can cause harmful neurological effects on infants and young children, including attention-related behavioral problems, decreased cognitive performance a
Details
Source
CPSC Consumer Product Recall
External ID
10288
Action Date
2025-05-29
Status
Recalled
Category
consumer_product
Product Description
This recall involves KICIMPRO kitchen faucets, model number KM800-01-06BN. The faucets are brushed nickel, single-handle
Company
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.
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 (Kaipingshikemuyulinweiyushiyeyouxiangongsi, of China, doing business as Amazon seller Kicimpro) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kaipingshikemuyulinweiyushiyeyouxiangongsi, of China, doing business as Amazon seller Kicimpro have FDA actions?
This is the only FDA action we have on record for Kaipingshikemuyulinweiyushiyeyouxiangongsi, of China, doing business as Amazon seller Kicimpro in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10288" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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