Wayfair Recalls Style Life Eleven Baby Loungers Due to Suffocation Risk and Fall Hazard; Violation of Federal Regulations for Infant Sleep Products; Sold Exclusively on Wayfair.com by Bespoke Clothing Valley (Royalbelle) through Zoomie Kids (Recall Alert)
Official recall recorded by the U.S. Consumer Product Safety Commission.
The hazard
The recalled baby loungers violate the federal safety regulations for Infant Sleep Products because the sleeping pad is too thick, posing a suffocation hazard; an infant could fall out of an enclosed opening at the sides of the lounger or become entrapped; and the sides are too low to contain the infant and the loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants.
What to do
Consumers should stop using the recalled baby loungers immediately and contact Wayfair for information on how to dispose of the product to obtain a full refund. Wayfair is contacting all known purchasers directly.
Brands named
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAVOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-0012026-05-08
- FDAVOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-0002026-03-25
- FDASemaglutide Inj, 2mg x 10, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-07.2026-02-26
- FDASemaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-001-062026-02-26
- FDATirzepatide Inj, 15mg x 4, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-002-04.2026-02-26
- FDATirzepatide Inj, 10mg, Sterile Multi-Dose Vial, Rx only, Nomida, 25055 W Valley Pkwy, Suite 106, Olathe, KS 66061, NDC 84223-002-03.2026-02-26
- FDAArtelon FlexBand Plus Ref: 41054 & 410572026-02-06
- FDAArtelon FlexBand Dynamic Matrix Ref: 310572026-02-06
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