Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa
- Recalling company
- Penner Patient Care, Inc.
- Product
- Penner Pacific Bathing Spa, Model Numbers 860010-1L
- 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
- 26 units
- Lot / codes
- UDI-DI: 0085007365409; Serial Numbers: 07246737902 10236603401 10226407101 03236488101 03246677601 08226379901 08226385601 12236632601 07226353601 08236572201 04246696501 01256844001 12246811601 06226337201 07236557301 09236582001 02246663101 09246761901 08226369401 08226374601 01246644601 04246691701 08246756001 10236600001 04256958001 04256952001
- Company location
- Aurora, NE
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1508-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1508-2026 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.