Penner Patient Care, Inc.: Medical Device Recall in 2026 - (Recall #: Z-1505-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2

Product Classification:

Class III

Date Initiated: August 13, 2025

Date Posted: March 18, 2026

Recall Number: Z-1505-2026

Event ID: 98396

Reason for Recall:

The device does not bear a unique device identifier.

Status: Ongoing

Product Quantity: 25 units

Code Information:

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

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated