Penner Pacific Bathing Spa Recall
Penner Pacific Bathing Spa, Model Numbers 360020-1P
Updated August 13, 2025
Penner Pacific Bathing Spa Model 360020-1P is being recalled because it lacks a unique device identifier required by regulation. This is a labeling and tracking issue with no reported safety hazard to users.
Is the Penner Patient Care, Inc. recalled? Yes. This product was recalled by FDA on August 13, 2025. Details below.
What is recalled
Penner Pacific Bathing Spa, Model Number 360020-1P
Am I affected
You're affected if you own or operate a Penner Pacific Bathing Spa with Model Number 360020-1P.
What to do right now
Contact Penner Patient Care, Inc. directly to report your device and receive guidance on the firm's voluntary recall process. No additional steps are required unless the manufacturer instructs otherwise.
The hazard
The device does not bear a unique device identifier.
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-1502-2026
- Classification
- Class III
- Recalled
- August 13, 2025
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