FDAAugust 13, 2025device

Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The device does not bear a unique device identifier.

What to do

FDA enforcement status: Ongoing

Brands named

penner patient carepennerpenner patient

UPCs

0085007365407

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL — Recall Details · AllClear