Nest Swing Egg Chairs
Summary
CPSC recall: Nest Swing Egg Chairs. By Marshalls, T.J. Maxx, HomeGoods and Homesense stores nationwide from December 2018 through April 2022 for between $300 and $350.. Hazard: The chairs can tip over or collapse when a consumer is seated in the chair, posing a fall hazard.. Remedy: Consumers should immediately stop using the recalled egg chairs and return them to any Marshalls, T.J. Maxx, HomeGoods, or Homesense stores for their choice of either a full refund or a refund in the form of a store
Details
Source
CPSC Consumer Product Recall
External ID
9329
Action Date
2022-06-16
Status
Recalled
Category
consumer_product
Product Description
This recall involves nest swing egg chairs sold under the Tommy Bahama and Martha Stewart brands. The chairs have a meta
Context & Analysis
This is a unclassified recall.
This was one of 17 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 (Marshalls, T.J. Maxx, HomeGoods and Homesense stores nationwide from December 2018 through April 2022 for between $300 and $350.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Marshalls, T.J. Maxx, HomeGoods and Homesense stores nationwide from December 2018 through April 2022 for between $300 and $350. have FDA actions?
This is the only FDA action we have on record for Marshalls, T.J. Maxx, HomeGoods and Homesense stores nationwide from December 2018 through April 2022 for between $300 and $350. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9329" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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