FDA Medical devices recall ·
Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000 recall
- Recall number
- Z-2882-2026
- Date
- (initiated May 15, 2024)
- Company / brand
- Happiest Baby, Inc
11390 W Olympic Blvd Ste 450, Los Angeles, CA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 4 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000
Why was it recalled?
This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot Code: 9677201861339395 3023201712722817 8714212700040040 0069193417621270
Distribution
US Nationwide distribution in states of PA, WA, CA, NJ.
States: California New Jersey Pennsylvania Washington
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2882-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.