TheKiddoSpace Print and Cursive Handwriting Kits
Summary
CPSC recall: TheKiddoSpace Print and Cursive Handwriting Kits. By Online at TheKiddoSpaceStore.com and Amazon.com from February 2024 through February 2025 for between $25 and $50.. Hazard: The pens in the recalled children's handwriting kits contain levels of lead in the nib that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.. Remedy: Consumers should stop using the recalled handwriting kits immediately, take the pens and ref
Details
Source
CPSC Consumer Product Recall
External ID
10636
Action Date
2026-02-26
Status
Recalled
Category
consumer_product
Product Description
This recall involves two different types of TheKiddoSpace-branded handwriting practice kits sold with or without a carry
Context & Analysis
This is a unclassified recall.
This was one of 35 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 (Online at TheKiddoSpaceStore.com and Amazon.com from February 2024 through February 2025 for between $25 and $50.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Online at TheKiddoSpaceStore.com and Amazon.com from February 2024 through February 2025 for between $25 and $50. have FDA actions?
This is the only FDA action we have on record for Online at TheKiddoSpaceStore.com and Amazon.com from February 2024 through February 2025 for between $25 and $50. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10636" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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