Medical device recalls

Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030…

Recall date
August 13, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1503-2026
FDA classification
Class III
Brand / firm
Penner Patient Care, Inc.
Sold / distributed
US Nationwide distribution.

Why it was recalled

The device does not bear a unique device identifier.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 360030-1CTS, 360030-XCTS, 3600301-CTS, 360030-XCE, 360030-1CT, 360030-1CE, 36030-XCT

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