Penner Patient Care, Inc.: Medical Device Recall in 2026 - (Recall #: Z-1508-2026)

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 860010-1L

Product Classification:

Class III

Date Initiated: August 13, 2025

Date Posted: March 18, 2026

Recall Number: Z-1508-2026

Event ID: 98396

Reason for Recall:

The device does not bear a unique device identifier.

Status: Ongoing

Product Quantity: 26 units

Code Information:

UDI-DI: 0085007365409; Serial Numbers: 07246737902 10236603401 10226407101 03236488101 03246677601 08226379901 08226385601 12236632601 07226353601 08236572201 04246696501 01256844001 12246811601 06226337201 07236557301 09236582001 02246663101 09246761901 08226369401 08226374601 01246644601 04246691701 08246756001 10236600001 04256958001 04256952001

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated