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FDA DeviceClass IIINotable

FDA Recall: Penner Pacific Bathing Spa, Model Numbers 360020-1EP

Date: 2026-03-18
Brand: Penner Patient Care, Inc.
Category: Medical Device
FDA Class: Class III

Description

The device does not bear a unique device identifier.

Hazard

The device does not bear a unique device identifier.

Remedy

10 units

View original recall →
FDA Recall: Penner Pacific Bathing Spa, Model Numbers 360020-1EP | RecallWatch