Recall
FDAHealthAugust 13, 2025

Penner Patient Care, Inc. — Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL

⚠️ The device does not bear a unique device identifier.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
August 13, 2025

US Nationwide distribution.

What's affected?

Product
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
Lot code
UDI-DI: 0085007365407; Serial Numbers: 11154213601 10205645901 10205645902 04226315103 09236585801 09185126701 06195328701 12236630901 03236489605 02226270301 02226270302 02256898401 03164326301 06216124001 11152429201

Additional details

UDI-DI: 0085007365407; Serial Numbers: 11154213601 10205645901 10205645902 04226315103 09236585801 09185126701 06195328701 12236630901 03236489605 02226270301 02226270302 02256898401 03164326301 06216124001 11152429201

What should I do?

Recommended action

Class III recall. Voluntary: Firm initiated Quantity affected: 15 units.

View original FDA notice →

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