FDA recall Z-1503-2026

Penner Patient Care, Inc. · Class III · device

Product

Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 360030-1CTS, 360030-XCTS, 3600301-CTS, 360030-XCE, 360030-1CT, 360030-1CE, 36030-XCT

Reason for recall

The device does not bear a unique device identifier.

Distribution

US Nationwide distribution.

Key facts

Status: Ongoing
Initiation date: 2025-08-13
Report date: 2026-03-18
Voluntary/Mandated: Voluntary: Firm initiated
Location: Aurora, NE, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1503-2026