FDA-Device2026-03-18Class IIIMISBRANDING
Penner Pacific Bathing Spa recalled for missing unique device identifier
What this means
Certain Penner Pacific Bathing Spa models do not have a unique device identifier (UDI) as required by FDA regulations. This affects 206 units with specific serial numbers distributed nationwide. No injuries have been reported.
- Check if your bathing spa serial number matches the recall list
- Contact Penner Patient Care, Inc. for instructions on how to proceed
- Do not use the device if your serial number is affected until you receive guidance
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
206 units
Manufactured in
101 Grant St, N/A, Aurora, NE, United States
Products
Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 360030-1CTS, 360030-XCTS, 3600301-CTS, 360030-XCE, 360030-1CT, 360030-1CE, 36030-XCT
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1503-2026Want us to check the next one for you?
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