Penner Patient Care, Inc.: Medical Device Recall in 2026 - (Recall #: Z-1499-2026)

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 350010-1, 350000-2, 350010-X

Product Classification:

Class III

Date Initiated: August 13, 2025

Date Posted: March 18, 2026

Recall Number: Z-1499-2026

Event ID: 98396

Reason for Recall:

The device does not bear a unique device identifier.

Status: Ongoing

Product Quantity: 21 units

Code Information:

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

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated