CLASS II ONGOING Device recall · Reported 12 Aug 2026 · FDA Enforcement Report

Pre-loved SNOO Smart Sleeper recalled by Happiest Baby

Happiest Baby is recalling Pre-loved SNOO Smart Sleeper, distributed nationwide in the US. The recall was initiated on 15 May 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: 9677201861339395 3023201712722817 8714212700040040 0069193417621270
Quantity recalled4 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-2882-2026
FDA event ID
99365
Recalling firm
Happiest Baby, Los Angeles, CA
Classification
Class II
Status
Ongoing
Recall initiated
15 May 2024
FDA classified
4 Aug 2026
Reported
12 Aug 2026
Type
Voluntary: Firm initiated
Customers notified by
Other
Reason category
Other Reasons

Timeline

15 May 2024Recall initiated by company
4 Aug 2026Classified by FDA+811 days
12 Aug 2026Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

US Nationwide distribution in states of PA, WA, CA, NJ.

Nationwide CaliforniaNew JerseyPennsylvaniaWashington

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot Code: 9677201861339395 3023201712722817 8714212700040040 0069193417621270

Where was it sold?

US Nationwide distribution in states of PA, WA, CA, NJ.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Happiest Baby

All 3
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IISNOO Sleep Sack, X-Large recalled by Happiest BabyHappiest BabyOtherNationwide
DeviceCLASS IISNOO Sleep Sack, X-Small recalled by Happiest BabyHappiest BabyOtherNationwide

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