Penner Pacific Bathing Spa — Class III medical device recall Z-1502-2026
Ongoing recall by Penner Patient Care, Inc., reported 2026-03-18, distributed nationwide. The device does not bear a unique device identifier.
| Recall number | Z-1502-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Penner Patient Care, Inc., Aurora, NE, United States |
| Recall initiated | 2025-08-13 |
| Classified | 2026-03-09 |
| Reported by FDA | 2026-03-18 |
| Distributed | Nationwide (US) |
| Quantity | 45 units |
| Serial numbers | 01142094001, 01192959801, 01192960801, 01192960802, 01203118301, 01226256901, 01226259601, 02192976301, 02246673801, 03192998301, 03203147601, 03203148701, 03216060801, 03216065101, 03246682701, 03256938801, 05182864901, 05216107301, 05216107302, 05216107303, 05216107304, 05216107305, 05216108301, 05216108302, 05216113101 and 20 more |
| Model numbers | 360020-1P |
Product
Penner Pacific Bathing Spa, Model Numbers 360020-1P
Reason for recall
The device does not bear a unique device identifier.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1502-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.