Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
FDA Recall #Z-1505-2026 — Class III — August 13, 2025
Product Description
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
Reason for Recall
The device does not bear a unique device identifier.
Recalling Firm
Penner Patient Care, Inc. — Aurora, NE
Classification
Class III — Not likely to cause adverse health consequences.
Product Type
Devices
Product Quantity
25 units
Distribution
US Nationwide distribution.
Code Information
UDI-DI: 0085007365406; Serial Numbers: 11185169701 01205459101 09236589001 08226376601 05236519007 07154096101 09185123501 09205645001 06216123501 06216123502 06216123503 04246695301 05205559701 05226325001 05226333501 03216074601 03216074602 03216074603 03216074604 04195277301 04216084201 05246707001 06195314201 03256918201 03256945401
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated