Penner Pacific Bathing Spa — Class III medical device recall Z-1505-2026
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-1505-2026 |
|---|---|
| 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 | 25 units |
| UPC / GTIN / UDI-DI | 00085007365406 |
| Serial numbers | 01205459101, 03216074601, 03216074602, 03216074603, 03216074604, 03256918201, 03256945401, 04195277301, 04216084201, 04246695301, 05205559701, 05226325001, 05226333501, 05236519007, 05246707001, 06195314201, 06216123501, 06216123502, 06216123503, 07154096101, 08226376601, 09185123501, 09205645001, 09236589001, 11185169701 |
| Model numbers | 390010-1, 390010-2, 390010-X |
Product
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
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-1505-2026. 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.