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Medical Device

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

Recall date: 2026-03-18 · Source: FDA_DEVICE
Product
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
Reason for recall
The device does not bear a unique device identifier.
Units affected
15 units
Description
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
View official recall notice →