FDAClass IIIMarch 18, 2026

Penner Pacific Bathing Spa recall

Penner Pacific Bathing Spa, Model Numbers 360020-1EP

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: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803

Product
Penner Pacific Bathing Spa, Model Numbers 360020-1EP
Recalling firm
Penner Patient Care, Inc.
Quantity
10 units
Distribution
US Nationwide distribution.
Recall date
March 18, 2026
Classification
Class III
Status
Ongoing
Agency
FDA (device)
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