# FDA recall Z-1500-2026

> **Penner Patient Care, Inc.** · Class III · device recall initiated 2025-08-13.

## Product

Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-2WL, 360010-X, 370000-XW, 360010-2W, 362010-2, 360010, 37000-XWL, 362010-X, 362010-XL, 362010-1L, 360010-XL, 37000-1W, 360010-XW, 3700000-1W, 362010-2L, 36010-XWT, 370000-1L, 360010-2WT, 360000-1, 360010-XWSB, 360010-XLSB

## Reason for recall

The device does not bear a unique device identifier.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1500-2026
- **Recalling firm:** Penner Patient Care, Inc.
- **Classification:** Class III
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-13
- **Report date:** 2026-03-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Aurora, NE, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1500-2026

## Citation

> AI Analytics. FDA recall Z-1500-2026. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-1500-2026. Source: US FDA. Licensed CC0.

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