FDA-Device2026-03-18Class IIIMISBRANDING
Penner Pacific Bathing Spa recalled for missing unique device identifier
OTHERNationwide distribution
Check your Penner Pacific Bathing Spa serial number
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
Hazard
The device does not bear a unique device identifier.
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-1503-2026More Penner Patient Care, Inc. recalls
- FDA-Device2026-03-18Penner Pacific Bathing Spa Model 360020-1P recalled for missing unique device identifier
- FDA-Device2026-03-18Penner Pacific Bathing Spa, Model Numbers 360020-1EP
- FDA-Device2026-03-18Penner Pacific Bathing Spa recalled for missing unique device identifier
- FDA-Device2026-03-18Penner Pacific Bathing Spa recalled for missing unique device identifier
- FDA-Device2026-03-18Penner Pacific Bathing Spa recalled for missing unique device identifier
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