Class III
Medical Device Recall: Penner Pacific Bathing Spa, Model Numbers 360020-1EP
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
10 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1501-2026
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.