Penner Patient Care, Inc.: Medical Device Recall in 2026 - (Recall #: Z-1501-2026)

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 360020-1EP

Product Classification:

Class III

Date Initiated: August 13, 2025

Date Posted: March 18, 2026

Recall Number: Z-1501-2026

Event ID: 98396

Reason for Recall:

The device does not bear a unique device identifier.

Status: Ongoing

Product Quantity: 10 units

Code Information:

UDI-DI: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated