Penner Pacific Bathing Spa, Model Numbers 360020-1EP
FDA Recall #Z-1501-2026 — Class III — August 13, 2025
Product Description
Penner Pacific Bathing Spa, Model Numbers 360020-1EP
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
10 units
Distribution
US Nationwide distribution.
Code Information
UDI-DI: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated