FDA DeviceClass IIINotable

FDA Recall: Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 36

Name: FDA Recall: Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 36
Brand: Penner Patient Care, Inc.

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

158 units

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