Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
FDA Recall #Z-1506-2026 — Class III — August 13, 2025
Product Description
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
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
15 units
Distribution
US Nationwide distribution.
Code Information
UDI-DI: 0085007365407; Serial Numbers: 11154213601 10205645901 10205645902 04226315103 09236585801 09185126701 06195328701 12236630901 03236489605 02226270301 02226270302 02256898401 03164326301 06216124001 11152429201
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated