Class III

Medical Device Recall: Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2

Penner Patient Care, Inc. · August 13, 2025

Reason for Recall

The device does not bear a unique device identifier.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

25 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1505-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Penner Patient Care, Inc. Medical Device Recall: Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2 | SafeCheck