Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa
- Recalling company
- Penner Patient Care, Inc.
- Product
- Penner Pacific Bathing Spa, Model Numbers 360020-1EP
- Reason
- The device does not bear a unique device identifier.
- Classification
- Class III – not likely to cause adverse health consequences
- Recall date
- Aug 13, 2025
- Reported
- Mar 18, 2026
- Distribution
- US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 10 units
- Lot / codes
- UDI-DI: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803
- Company location
- Aurora, NE
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1501-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1501-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.