Penner Pacific Bathing Spa recall
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
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: 0085007365406; Serial Numbers: 11185169701 01205459101 09236589001 08226376601 05236519007 07154096101 09185123501 09205645001 06216123501 06216123502 06216123503 04246695301 05205559701 05226325001 05226333501 03216074601 03216074602 03216074603 03216074604 04195277301 04216084201 05246707001 06195314201 03256918201 03256945401
- Product
- Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
- Recalling firm
- Penner Patient Care, Inc.
- Quantity
- 25 units
- Distribution
- US Nationwide distribution.
- Recall date
- March 18, 2026
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (device)