Penner Pacific Bathing Spa recall
Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
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: 0085007365400; Serial Numbers: 06020315401 08010223607 04205543401 05246707501 05246707502 02195222101 11216213301 09185118801 10216206001 10216206002 11216222201 11216222202 05246717201 02195236901 11195422801 01246647601 01246656501 04205544901 12205685701 09236590301 11195432401
- Product
- Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
- Recalling firm
- Penner Patient Care, Inc.
- Quantity
- 21 units
- Distribution
- US Nationwide distribution.
- Recall date
- March 18, 2026
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (device)