Penner Patient Care, Inc.: Medical Device Recall in 2026 - (Recall #: Z-1506-2026)

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 560010-2L, 560010-XL, 560010-1L, 560010-XL

Product Classification:

Class III

Date Initiated: August 13, 2025

Date Posted: March 18, 2026

Recall Number: Z-1506-2026

Event ID: 98396

Reason for Recall:

The device does not bear a unique device identifier.

Status: Ongoing

Product Quantity: 15 units

Code Information:

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

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated