Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa
- Recalling company
- Penner Patient Care, Inc.
- Product
- Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
- 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
- 21 units
- Lot / codes
- UDI-DI: 0085007365400; Serial Numbers: 06020315401 08010223607 04205543401 05246707501 05246707502 02195222101 11216213301 09185118801 10216206001 10216206002 11216222201 11216222202 05246717201 02195236901 11195422801 01246647601 01246656501 04205544901 12205685701 09236590301 11195432401
- Company location
- Aurora, NE
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1499-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1499-2026 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.