FDA-Device2026-03-18Class IIIMISBRANDING
Penner Pacific Bathing Spa recalled for missing device identifier
OTHERNationwide distribution
Check your Penner Pacific Bathing Spa serial number
Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa models because they do not have the required unique device identifier (UDI) label. This makes it difficult to track the device for safety purposes. No injuries have been reported.
- Check if your bathing spa serial number matches the list provided by the FDA
- Contact Penner Patient Care, Inc. for instructions on obtaining the proper identifier or replacement
- Do not discard the device; wait for further guidance from the manufacturer
Hazard
The device does not bear a unique device identifier.
Sold states
US Nationwide distribution.
Affected count
15 units
Manufactured in
101 Grant St, N/A, Aurora, NE, United States
Products
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1506-2026More 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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