FDA-Device2026-03-18Class IIIMISBRANDING
Penner Pacific Bathing Spa recalled for missing device identifier
What this means
Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa models (390010-1, 390010-X, 390010-2) because they do not have the required unique device identifier. This is a regulatory compliance issue. About 25 units are affected.
- Check if your bathing spa serial number matches the list provided by the FDA
- Contact Penner Patient Care, Inc. for instructions on remedy or replacement
- Do not use the spa if your serial number is on the recall list
The agency's original wording
Hazard
The device does not bear a unique device identifier.
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution.
Affected count
25 units
Manufactured in
101 Grant St, N/A, Aurora, NE, United States
Products
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1505-2026Want us to check the next one for you?
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