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 federal regulations. This affects 643 units with specific serial numbers. No injuries have been reported.
- Check if your bathing spa serial number matches the FDA recall list
- Contact Penner Patient Care, Inc. for instructions on next steps
- Do not discard the device until you receive guidance from the manufacturer
Hazard
The device does not bear a unique device identifier.
Sold states
US Nationwide distribution.
Affected count
643 units
Manufactured in
101 Grant St, N/A, Aurora, NE, United States
Products
Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-2WL, 360010-X, 370000-XW, 360010-2W, 362010-2, 360010, 37000-XWL, 362010-X, 362010-XL, 362010-1L, 360010-XL, 37000-1W, 360010-XW, 3700000-1W, 362010-2L, 36010-XWT, 370000-1L, 360010-2WT, 360000-1, 360010-XWSB, 360010-XLSB
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1500-2026More 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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