Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The device does not bear a unique device...

Date: August 13, 2025
Company: Penner Patient Care, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Penner Patient Care, Inc. directly.

Affected Products

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

Quantity: 206 units

Why Was This Recalled?

The device does not bear a unique device identifier.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Penner Patient Care, Inc.

Penner Patient Care, Inc. has 10 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report