FDA-Device2026-03-18Class IIIMISBRANDING
Penner Pacific Bathing Spa recalled for missing unique device identifier
What this means
Certain Penner Pacific Bathing Spa units (Models 760010-1 and 770010-1) were distributed without a required unique device identifier (UDI) label. This label helps health authorities track and manage medical devices. The FDA has identified 190 affected units by serial number.
- Find your spa's serial number on the device
- Check if it matches any of the recalled serial numbers listed in the FDA notice
- If your spa is affected, contact Penner Patient Care, Inc. for instructions
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
190 units
Manufactured in
101 Grant St, N/A, Aurora, NE, United States
Products
Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1507-2026Want us to check the next one for you?
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