Official recall notice
FDA DeviceClass IIINotable
FDA Recall: Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
- Recall date
- 2026-03-18
- Category
- Medical Device
- FDA class
- Class III
Why it was recalled
Hazard
The device does not bear a unique device identifier.
Recommended action
What to do
15 units
Product description
The device does not bear a unique device identifier.