Penner Pacific Bathing Spa recall
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
Why was Penner Pacific Bathing Spa recalled?
The device does not bear a unique device identifier.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 0085007365407; Serial Numbers: 11154213601 10205645901 10205645902 04226315103 09236585801 09185126701 06195328701 12236630901 03236489605 02226270301 02226270302 02256898401 03164326301 06216124001 11152429201
- Product
- Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
- Recalling firm
- Penner Patient Care, Inc.
- Quantity
- 15 units
- Distribution
- US Nationwide distribution.
- Recall date
- March 18, 2026
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (device)