Penner Pacific Bathing Spa — Class III medical device recall Z-1507-2026
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-1507-2026 |
|---|---|
| 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 | 190 units |
| Serial numbers | 01205470701, 01205470801, 01205479701, 01205488401, 01216010402, 01226251401, 01226251402, 01226251403, 01226262601, 01236457201, 01236457202, 01236461401, 01246639801, 01246651201, 01246651202, 01246654601, 01256819701, 01256858401, 01256858402, 02205500701, 02205500702, 02205500703, 02205504501, 02205504901, 02216027601 and 163 more |
| Model numbers | 760010-1, 770010-1 |
Product
Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1
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-1507-2026. 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.