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

Penner Patient Care, Inc.: Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X

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

Read the official notice at FDA (device) →

Share on XFacebookRedditEmail

Get alerts for Penner Patient Care

Guides: Which agency handles which recall (FDA vs USDA vs CPSC vs NHTSA)

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 350010-1, 350000-2, 350010-X
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: 0085007365400; Serial Numbers: 06020315401 08010223607 04205543401 05246707501 05246707502 02195222101 11216213301 09185118801 10216206001 10216206002 11216222201 11216222202 05246717201 02195236901 11195422801 01246647601 01246656501 04205544901 12205685701 09236590301 11195432401
Product quantity
21 units
Voluntary mandated
Voluntary: Firm initiated
City
Aurora
State
NE
Country
United States
Event id
98396
Free daily digest + "My products" watchlist

Get the daily digest, and tell us what to watch. Everything is optional except your email.

Free allergen alerts:

Categories:

Privacy: we store only what you enter here, use it only to send recall alerts you asked for, never sell or share it, and you can unsubscribe anytime. Double opt-in: we will email you a confirmation link before sending anything; alerts start only after you confirm. Every email has unsubscribe and manage-watchlist links.