⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Penner Patient Care, Inc.: Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2

Medical DevicesSource: FDA (device) · Date: 2026-03-18

Read the official notice at FDA (device) →

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The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
Penner Patient Care, Inc.
Product
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
Reason / hazard
The device does not bear a unique device identifier.
Classification
Class III
Status
Ongoing
Distribution / sold at
US Nationwide distribution.
Recall initiated
2025-08-13
Code info
UDI-DI: 0085007365406; Serial Numbers: 11185169701 01205459101 09236589001 08226376601 05236519007 07154096101 09185123501 09205645001 06216123501 06216123502 06216123503 04246695301 05205559701 05226325001 05226333501 03216074601 03216074602 03216074603 03216074604 04195277301 04216084201 05246707001 06195314201 03256918201 03256945401
Product quantity
25 units
Voluntary mandated
Voluntary: Firm initiated
City
Aurora
State
NE
Country
United States
Event id
98396
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