Inclined sleeper accessory included with Kolcraft Cuddle 'n Care 2-in-1 Bassinet & Incline Sleepers and Preferred Positi
Summary
CPSC recall: Inclined sleeper accessory included with Kolcraft Cuddle 'n Care 2-in-1 Bassinet & Incline Sleepers and Preferred Position 2-in-1 Bassinet & Incline Sleepers. By Juvenile product stores and mass merchandisers nationwide from March 2011 through December 2017 for about $140.. Hazard: Infant fatalities have been reported with other manufacturers' inclined sleep products, after the infants rolled from their back to their stomach or side, or under other circumstances.. Remedy: Consumers
Details
Source
CPSC Consumer Product Recall
External ID
9054
Action Date
2021-05-05
Status
Recalled
Category
consumer_product
Product Description
This recall involves the inclined sleeper accessory sold with the Kolcraft Cuddle 'n Care 2-in-1 Bassinet & Incline Slee
Context & Analysis
This is a unclassified recall.
This was one of 12 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 (Juvenile product stores and mass merchandisers nationwide from March 2011 through December 2017 for about $140.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Juvenile product stores and mass merchandisers nationwide from March 2011 through December 2017 for about $140. have FDA actions?
This is the only FDA action we have on record for Juvenile product stores and mass merchandisers nationwide from March 2011 through December 2017 for about $140. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9054" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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