RecallHawk

Peg Perego Tatamia 3-in-1 Recliner, Swings and High Chairs

Peg Perego SPA, of Italy

Summary

CPSC recalled Peg Perego Tatamia 3-in-1 Recliner, Swings and High Chairs by Peg Perego SPA, of Italy. Hazard: The 3-in-1 products pose a suffocation risk because they were marketed for infant sleep, and they have an incline angle greater than 10 degrees, in violation of the Infant Sleep Products Rule and Safe Sleep for Babies Act. In addition, the products fail to meet mandatory warning requirements under the high chair standard.. Remedy: Consumers should immediately stop using the recalled products and contact Peg Perego for a full refund. Consumers should contact Peg Perego for a prepaid shipping label and packaging to send the products back to Peg Perego. Peg Perego and Amazon are contacting all known purchasers directly..

Details

Source

cpsc

External ID

25706

Action Date

2025-06-26

Status

Ongoing

Category

product

Product Description

This recall involves Peg Perego Tatamia recliners, swings and high chairs. The products convert from a recliner to a high chair and to an unpowered infant swing, and they were sold in "Ice" (gray) color with model number IMTATANA01BL73. The top of the padded leather seat has the brand name "Peg Perego" printed on it. In high chair mode "Peg Perego" is printed on the front of the tray. The adjustable side of the product has "tatamia" printed on it. Only products manufactured on or after June 23, 2022, and/or purchased on or after November 12, 2022, are included in this recall. The manufacture date in YYYY/MM/DD format and model number can be found on the base of the product.

Context & Analysis

Peg Perego SPA, of Italy has 4 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

How often does Peg Perego SPA, of Italy have FDA actions?

Peg Perego SPA, of Italy has 4 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for product

Related Actions