Z-0458-06

The First Years Cool Animal Teether/Fish, Zebra and Dinosaur designs Style #Y1473

Name: Z-0458-06 The First Years Cool Animal Teether/Fish, Zebra and Dinosaur designs Style #Y1473
Creator: RC2 Brands Inc., The First Years
Published: 2006-01-25
License: https://open.fda.gov/license/

TOMY International / initiated 2006-01-25 / Terminated

FDA source

RC2 Brands Inc., The First Years began a recall of The First Years Cool Animal Teether/Fish, Zebra and Dinosaur designs Style #Y1473 on 2006-01-25. The reason FDA records is "Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0458-06
Status: Terminated
Initiated: 2006-01-25
Posted: 2006-02-09
Terminated: 2006-08-10
Recalling firm: TOMY International
Product: The First Years Cool Animal Teether/Fish, Zebra and Dinosaur designs Style #Y1473
Product code: KKO Ring, Teething, Fluid-Filled
Reason for recall: Liquid Filled Infant teething ring contaminated with Pseudomonas aeruginosa and Pseudomonas putida
FDA root cause: Other
Action: RC2/The First Years initiated recall by email with recall letter on 1/27 /06. Buyers will advise retail stores to remove product from retail shelves and return to First Years for replacement. The firm is posting the recall to their website: www.thefirstyears.com. A Press Release was issued to AP on 1/27/05.
Distribution: Nationwide Foreign: Canada, UK, Australia, Mexico
Product codes and lots: All codes

Product code KKO

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)