Z-1501-2026 Class III Ongoing
FDA device recall Z-1501-2026 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: 10 units.
Recall details
- Product Type
- Devices
- Report Date
- Mar 18, 2026
- Initiation Date
- Aug 13, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10 units
Product description
Penner Pacific Bathing Spa, Model Numbers 360020-1EP
Reason for recall
The device does not bear a unique device identifier.
Distribution pattern
US Nationwide distribution.
Code information
UDI-DI: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1501-2026
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026