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 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
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
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-1500-2026Want us to check the next one for you?
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