FDA Device recall Z-0766-2023
Lamaze Chill Teether, Fluid-Filled Teething Ring, Model No. Y5288L
- FDA Device
- Class II
- ongoing
- Published 2022-12-28
On 2022-12-28 the FDA classified a Class II recall of Lamaze Chill Teether, Fluid-Filled Teething Ring, Model No. Y5288L by Tomy International, citing affected lots of the product are being recalled due to potential microbial growth in the fluid inside the device. if a compromised product is used by a child with a weakened immun….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0766-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-12-02 |
| Published | 2022-12-28 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Tomy International |
| Distribution | US |
Product
Lamaze Chill Teether, Fluid-Filled Teething Ring, Model No. Y5288L
Reason
Affected lots of the product are being recalled due to potential microbial growth in the fluid inside the device. if a compromised product is used by a child with a weakened immune system, an infection or other illness could occur.
Identifiers
| code_info | UDI-DI B268Y5288L0 Lot Numbers E1920ALP01 and K1920ALP01 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0766-2023%22
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