Penner Pacific Bathing Spa — Class III medical device recall Z-1506-2026
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-1506-2026 |
|---|---|
| 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 | 15 units |
| Serial numbers | 02226270301, 02226270302, 02256898401, 03164326301, 03236489605, 04226315103, 06195328701, 06216124001, 09185126701, 09236585801, 10205645901, 10205645902, 11152429201, 11154213601, 12236630901 |
| Model numbers | 560010-1L, 560010-2L, 560010-XL |
Product
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
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-1506-2026. 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.