Penner Pacific Bathing Spa, Model Numbers 860010-1L
FDA Recall #Z-1508-2026 — Class III — August 13, 2025
Product Description
Penner Pacific Bathing Spa, Model Numbers 860010-1L
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
26 units
Distribution
US Nationwide distribution.
Code Information
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
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated