Z-1506-2026 Class III Ongoing
FDA device recall Z-1506-2026 was initiated by Penner Patient Care, Inc. on Aug 13, 2025 and is designated Class III. Reason for recall: The device does not bear a unique device identifier. The recall status is ongoing. Affected quantity: 15 units.
Recall details
- Product Type
- Devices
- Report Date
- Mar 18, 2026
- Initiation Date
- Aug 13, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 15 units
Product description
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
Reason for recall
The device does not bear a unique device identifier.
Distribution pattern
US Nationwide distribution.
Code information
UDI-DI: 0085007365407; Serial Numbers: 11154213601 10205645901 10205645902 04226315103 09236585801 09185126701 06195328701 12236630901 03236489605 02226270301 02226270302 02256898401 03164326301 06216124001 11152429201
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1506-2026
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026