Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
FDA Recall #Z-1499-2026 — Class III — August 13, 2025
Product Description
Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
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
21 units
Distribution
US Nationwide distribution.
Code Information
UDI-DI: 0085007365400; Serial Numbers: 06020315401 08010223607 04205543401 05246707501 05246707502 02195222101 11216213301 09185118801 10216206001 10216206002 11216222201 11216222202 05246717201 02195236901 11195422801 01246647601 01246656501 04205544901 12205685701 09236590301 11195432401
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated