Summary
The FDA issued a Class II for Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000 by Happiest Baby, Inc. Reason: This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution..
Details
Source
Device Recall
External ID
Z-2882-2026
Action Date
2026-08-12
Status
Ongoing
Category
device
Product Description
Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000
Lot/Code Info: Lot Code: 9677201861339395 3023201712722817 8714212700040040 0069193417621270
Quantity Affected: 4 units
Reason for Recall
This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution.
Distribution
US Nationwide distribution in states of PA, WA, CA, NJ.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-15
Company
Los Angeles, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 156 device recalls issued in the same week, part of 400 device-related FDA actions this month.
Happiest Baby, Inc has 2 FDA actions in our database, including 1 recall and 1 clearance.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Happiest Baby, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Happiest Baby, Inc have FDA actions?
Happiest Baby, Inc has 2 FDA actions in our database, including 1 recall and 1 device clearance.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2882-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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