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
SUNS International SS6291 Elevator Switch Recall
SUNS International is recalling SS6291 Solenoid Interlock Switches used in residential elevators because the switch can get stuck in a retracted position, …
SUNS SS6291 Solenoid Interlock Switches
Residential Elevators StrikeLock Door Lock Recall
Residential Elevators is recalling its StrikeLock hoistway door locking device, used on residential elevator landing doors. The defective lock can allow the …
Residential Elevators StrikeLock Hoistway Door Locking Device
BD PurPrep Povidone-Iodine Recall
BD PurPrep povidone-iodine sterile skin prep solution (25 applicators per carton) may not be sterile due to potential product contamination. Using a non-sterile …
CareFusion 213, LLC