Penner Pacific Bathing Spa — Class III medical device recall Z-1504-2026
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-1504-2026 |
|---|---|
| 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 | 158 units |
| Serial numbers | 01192960601, 01203113401, 01203116101, 01203116102, 01203116103, 01226261601, 01236449501, 01236449502, 01236457001, 01246648301, 01246648302, 01256823701, 01256834801, 01256838101, 01256852601, 02192979601, 02192981501, 02192981502, 02203131401, 02226266601, 02226270303, 02246665701, 02246671801, 02246672301, 03192987401 and 133 more |
| Model numbers | 36191-1A, 361910-1, 361910-1A, 361910-1I, 361910-2A, 361910-2I, 361910-X, 361910-XA, 361910-XI |
Product
Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X
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-1504-2026. 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.