FDA-Device2026-03-18Class IIIMISBRANDING
Penner Pacific Bathing Spa recalled for missing device identifier
OTHERNationwide distribution
Check your Penner Pacific Bathing Spa model
Penner Patient Care is recalling certain Penner Pacific Bathing Spa models because they do not have the required unique device identifier marked on them. This identifier helps track and manage the device if problems arise. No injuries have been reported.
- Check if your bathing spa matches one of the affected model numbers: 350010-1, 350000-2, or 350010-X
- If it does, verify the serial number against the list provided by the FDA
- Contact Penner Patient Care, Inc. for instructions on how to proceed
Hazard
The device does not bear a unique device identifier.
Sold states
US Nationwide distribution.
Affected count
21 units
Manufactured in
101 Grant St, N/A, Aurora, NE, United States
Products
Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1499-2026More 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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