Class IIIReported 2026-03-18

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

Recalled by Penner Patient Care, Inc.

Reason for Recall

The device does not bear a unique device identifier.

Recall Number

Z-1506-2026

Classification

Class III

Status

Ongoing

Category

device

Initiated

2025-08-13

Reported

2026-03-18

Distribution

US Nationwide distribution.

Code Info

UDI-DI: 0085007365407; Serial Numbers: 11154213601 10205645901 10205645902 04226315103 09236585801 09185126701 06195328701 12236630901 03236489605 02226270301 02226270302 02256898401 03164326301 06216124001 11152429201

Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.