Penner Pacific Bathing Spa — Class III medical device recall Z-1499-2026
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-1499-2026 |
|---|---|
| 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 | 21 units |
| Serial numbers | 01246647601, 01246656501, 02195222101, 02195236901, 04205543401, 04205544901, 05246707501, 05246707502, 05246717201, 06020315401, 08010223607, 09185118801, 09236590301, 10216206001, 10216206002, 11195422801, 11195432401, 11216213301, 11216222201, 11216222202, 12205685701 |
| Model numbers | 350000-2, 350010-1, 350010-X |
Product
Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-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-1499-2026. 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.