Home / Recalls / Medical Devices
Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
Recalled March 18, 2026 · FDA recall Z-1505-2026 · Penner Patient Care
Hazard
The device does not bear a unique device identifier. · FDA Class III
Units
25 units
Sold at
US Nationwide distribution.
Description
The device does not bear a unique device identifier.
Product
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
Manufacturer(s)
Penner Patient Care, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →