RecallHawk

Room & Board Natural Organic Latex and Latex and Spring Crib Mattresses

Restwell Mattress Co., of Eden Prairie, Minnesota

Summary

CPSC recall: Room & Board Natural Organic Latex and Latex and Spring Crib Mattresses. By Restwell Mattress Co., of Eden Prairie, Minnesota. Hazard: The recalled crib mattresses fail to comply with multiple provisions of the Federal Safety Standard for Crib Mattresses, including the firmness test and missing warnings and labels. The product poses a suffocation hazard to infants.. Remedy: Consumers should immediately stop using the crib mattresses and contact Room & Board to receive a full refund.

Details

Source

CPSC Consumer Product Recall

External ID

9688

Action Date

2023-08-10

Status

Recalled

Category

consumer_product

Product Description

This recall involves Room & Board brand crib mattresses, Natural Organic Latex and Spring Crib (Model no. 847564) and Na

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.

Restwell Mattress Co., of Eden Prairie, Minnesota 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 (Restwell Mattress Co., of Eden Prairie, Minnesota) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Restwell Mattress Co., of Eden Prairie, Minnesota have FDA actions?

Restwell Mattress Co., of Eden Prairie, Minnesota 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 "9688" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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