Happiest Baby — Class II medical device recall Z-2882-2026
Ongoing recall by Happiest Baby, Inc, reported 2026-08-12, distributed nationwide. This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to d
| Recall number | Z-2882-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Happiest Baby, Inc, Los Angeles, CA, United States |
| Recall initiated | 2024-05-15 |
| Classified | 2026-08-04 |
| Reported by FDA | 2026-08-12 |
| Distributed | Nationwide (US) |
| Quantity | 4 units |
| Lot numbers | 0069193417621270, 3023201712722817, 8714212700040040, 9677201861339395 |
| Model numbers | S1000 |
Product
Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000
Reason for recall
This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2882-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.