FDA DeviceClass IIINotable

FDA Recall: Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL

Name: FDA Recall: Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
Brand: Penner Patient Care, Inc.

Date: 2026-03-18

FDA Class: Class III

Description

The device does not bear a unique device identifier.

The device does not bear a unique device identifier.

15 units