Aderes bookcases
Summary
CPSC recall: Aderes bookcases. By HomeGoods and HomeGoods/Marshalls or T.J. Maxx combination stores nationwide from October 2021 through March 2022 for about $800.. Hazard: The recalled bookcases are unstable and can tip over if not anchored to the wall, posing tip-over and entrapment hazards that can result in death or injuries to children.. Remedy: Consumers should immediately stop using the recalled bookcases and contact TJX for either a full refund or a refund in the form of store gift card
Details
Source
CPSC Consumer Product Recall
External ID
9542
Action Date
2023-02-23
Status
Recalled
Category
consumer_product
Product Description
This recall involves all Aderes bookcases. The bell-shaped bookcases have a natural finish, measure 44" x 18" x 86" and
Context & Analysis
This is a unclassified recall.
This was one of 18 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 (HomeGoods and HomeGoods/Marshalls or T.J. Maxx combination stores nationwide from October 2021 through March 2022 for about $800.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does HomeGoods and HomeGoods/Marshalls or T.J. Maxx combination stores nationwide from October 2021 through March 2022 for about $800. have FDA actions?
This is the only FDA action we have on record for HomeGoods and HomeGoods/Marshalls or T.J. Maxx combination stores nationwide from October 2021 through March 2022 for about $800. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9542" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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