Recall
FDAHealthAugust 13, 2025

Penner Patient Care, Inc. — Penner Pacific Bathing Spa, Model Numbers 860010-1L

⚠️ 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 860010-1L
Lot code
UDI-DI: 0085007365409; Serial Numbers: 07246737902 10236603401 10226407101 03236488101 03246677601 08226379901 08226385601 12236632601 07226353601 08236572201 04246696501 01256844001 12246811601 06226337201 07236557301 09236582001 02246663101 09246761901 08226369401 08226374601 01246644601 04246691701 08246756001 10236600001 04256958001 04256952001

Additional details

UDI-DI: 0085007365409; Serial Numbers: 07246737902 10236603401 10226407101 03236488101 03246677601 08226379901 08226385601 12236632601 07226353601 08236572201 04246696501 01256844001 12246811601 06226337201 07236557301 09236582001 02246663101 09246761901 08226369401 08226374601 01246644601 04246691701 08246756001 10236600001 04256958001 04256952001

What should I do?

Recommended action

Class III recall. Voluntary: Firm initiated Quantity affected: 26 units.

View original FDA notice →

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