Penner Pacific Bathing Spa — Class III medical device recall Z-1500-2026
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-1500-2026 |
|---|---|
| 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 | 643 units |
| Serial numbers | 01192956501, 01192969601, 01195189901, 01195190001, 01195194601, 01195194602, 01195194701, 01195194702, 01195194801, 01195194802, 01195194803, 01195194804, 01195206601, 01195214901, 01203113501, 01203114101, 01205459301, 01205477401, 01205477402, 01205477403, 01205478501, 01205478601, 01205488501, 01205488601, 01205488701 and 475 more |
| Model numbers | 360000-1, 360010, 360010-1, 360010-1L, 360010-1W, 360010-1WT, 360010-1WTL, 360010-2, 360010-2L, 360010-2W, 360010-2WT, 360010-X, 360010-XL, 360010-XLSB, 360010-XW, 360010-XWSB, 360010-XWT, 360010-XWTL, 36010-XWT, 362010-1, 362010-1L, 362010-2, 362010-2L, 362010-X, 362010-XL and 10 more |
Product
Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-2WL, 360010-X, 370000-XW, 360010-2W, 362010-2, 360010, 37000-XWL, 362010-X, 362010-XL, 362010-1L, 360010-XL, 37000-1W, 360010-XW, 3700000-1W, 362010-2L, 36010-XWT, 370000-1L, 360010-2WT, 360000-1, 360010-XWSB, 360010-XLSB
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-1500-2026. 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.