← FDA ENFORCEMENT
Z-1501-2026Class III
Penner Patient Care, Inc.
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
Penner Patient Care, Inc.
Product type
Device
Status
Ongoing
Report date
2026-03-18
Distribution
US Nationwide distribution.
Firm state
NE
Product quantity
10 units
Initiated by
Voluntary: Firm initiated
Reason for recall
The device does not bear a unique device identifier.
Product description
Penner Pacific Bathing Spa, Model Numbers 360020-1EP
Code / lot info
UDI-DI: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →