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, Inc. is recalling certain Penner Pacific Bathing Spa units (Model 860010-1L) because they do not have the required unique device identifier marked on them. This identifier is needed for proper tracking and safety oversight. No injuries have been reported.
- Check if you own a Penner Pacific Bathing Spa Model 860010-1L with one of the affected serial numbers listed in the recall notice
- Contact Penner Patient Care, Inc. for instructions on how to remedy or return your unit
- Do not use the device if you cannot confirm your serial number is not on the recall list
Hazard
The device does not bear a unique device identifier.
Sold states
US Nationwide distribution.
Affected count
26 units
Manufactured in
101 Grant St, N/A, Aurora, NE, United States
Products
Penner Pacific Bathing Spa, Model Numbers 860010-1L
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1508-2026More 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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