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
Get free recall alerts
New Medical Devices recalls, the moment they post.
Free forever. Unsubscribe anytime. We never sell your data.
More Medical Devices recalls
Boston Scientific Rapid Refill Injection System Recall
Boston Scientific's Rapid Refill Continuous Injection System contains a recalled syringe component that may loosen or disconnect from the manifold. This can …
Boston Scientific Corporation
FARASTAR Ablation Generator Recall
Boston Scientific is replacing certain FARASTAR Pulsed Field Ablation generators that cannot work with the FARAPOINT catheter. If your generator has an …
Boston Scientific Corporation
Faradive Steerable Sheath Clear Recall
The Faradive Steerable Sheath Clear used in cardiac catheterization procedures may allow air to enter the bloodstream if the dilator is inserted incorrectly …
Boston Scientific Corporation