Medical device recalls

Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 3…

Recall date
August 13, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1504-2026
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 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X

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