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U.S. Department of Health and Human Services

Class 2 Device Recall Happiest Baby, Inc Preloved SNOO Smart Sleeper

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 Class 2 Device Recall Happiest Baby, Inc Preloved SNOO Smart Sleepersee related information
Date Initiated by FirmMay 15, 2024
Date PostedAugust 04, 2026
Recall Status1 Open3, Classified
Recall NumberZ-2882-2026
Recall Event ID 99365
Product Classification Infant supine sleep system - Product Code QTG
ProductHappiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000
Code Information Lot Code: 9677201861339395 3023201712722817 8714212700040040 0069193417621270
FEI Number 3030187577
Recalling Firm/
Manufacturer		 Happiest Baby, Inc
11390 W Olympic Blvd Ste 450
Los Angeles CA 90064-1607
For Additional Information ContactCustomer Care
310-4764440
Manufacturer Reason
for Recall		This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution.
FDA Determined
Cause 2		Reprocessing Controls
ActionHappiest Baby, Inc. did not issue a formal communication. Between the dates of May and July 2024, customers that noted issues with the product returned the affected unit and were provided a replacement.
Quantity in Commerce4 units
DistributionUS Nationwide distribution in states of PA, WA, CA, NJ.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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