FDA-Device2026-03-18Class IIIMISBRANDING
Penner Pacific Bathing Spa recalled for missing device identifier
What this means
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
The agency's original wording
Hazard
The device does not bear a unique device identifier.
Intended for
All ages
Illnesses reported
None reported
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-1508-2026Want us to check the next one for you?
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