Fresh Recalls

FDAClass II · Medical device · Recall Z-2882-2026 · Recalled August 12, 2026

Happiest Baby recall — Happiest Baby, Inc

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Happiest Baby
Company / brand
Happiest Baby
Lot / serial / date codes
Lot Code: 9677201861339395 3023201712722817 8714212700040040 0069193417621270
Distribution
US Nationwide distribution in states of PA, WA, CA, NJ.
Agency product description and boundaries

Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: This recall is retroactively being reported. Refurbished bassinets failed to meet quality standards prior to distribution.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Happiest Baby

3. Open the official notice or contact

Official recall ID
Z-2882-2026
Brand
Happiest Baby
Classification
Class II
Units affected
4 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Los Angeles, CA, United States
Firm address
11390 W Olympic Blvd Ste 450, 90064-1607

Identifying details (verbatim from the notice)

Product codes / lots
Lot Code: 9677201861339395 3023201712722817 8714212700040040 0069193417621270
Distribution
US Nationwide distribution in states of PA, WA, CA, NJ.
Firm notified the public via
Other
FDA event ID
99365
Recall initiated
May 15, 2024
FDA classified
August 4, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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