RecallHawk

HOFISH 10-Inch Hybrid Certi-PUR Certified Foam and Pocket Spring Mattresses

Vietnam Glory Home Furnishings Joint Stock Company, of Vietnam

Summary

CPSC recall: HOFISH 10-Inch Hybrid Certi-PUR Certified Foam and Pocket Spring Mattresses. By Vietnam Glory Home Furnishings Joint Stock Company, of Vietnam. Hazard: The mattresses fail to meet the mandatory federal flammability standard for mattresses, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled mattresses and contact HOFISH to receive a free fitted cover to put on the mattress to bring it into compliance with the federal standard..

Details

Source

CPSC Consumer Product Recall

External ID

9018

Action Date

2021-03-17

Status

Recalled

Category

consumer_product

Product Description

This recall involves HOFISH 10-Inch Hybrid Certi-PUR Certified Foam and Pocket Spring Mattresses sold in twin, twin XL,

Context & Analysis

This is a unclassified recall.

This was one of 6 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Vietnam Glory Home Furnishings Joint Stock Company, of Vietnam 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 (Vietnam Glory Home Furnishings Joint Stock Company, of Vietnam) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Vietnam Glory Home Furnishings Joint Stock Company, of Vietnam have FDA actions?

Vietnam Glory Home Furnishings Joint Stock Company, of Vietnam 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 "9018" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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