Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa
- Recalling company
- Penner Patient Care, Inc.
- Product
- Penner Pacific Bathing Spa, Model Numbers 360020-1P
- 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
- 45 units
- Lot / codes
- UDI-DI: 0085007365403; Serial Numbers: 11193097601 10216195501 10216195502 12193104901 06226342101 06226342102 06226342105 06226342107 03203148701 01226259601 10226410801 06246724701 10203210401 10203210402 05216113101 11193095401 01203118301 05216107301 05216107302 05216107303 05216107304 05216107305 05216108301 05216108302 06193030201 03203147601 09193066601 03216060801 07193052301 09236591501 02246673801 02192976301 03246682701 01192960801 01192960802 06236535501 08152390701 03216065101 05182864901 01142094001 11121856201 03192998301 01192959801 01226256901 03256938801
- Company location
- Aurora, NE
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1502-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1502-2026 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.