Penner Pacific Bathing Spa — Class III medical device recall Z-1503-2026
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-1503-2026 |
|---|---|
| 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 | 206 units |
| Serial numbers | 01162459901, 01192956301, 01192958901, 01192967301, 01192967401, 01203111201, 01203113001, 01203113002, 01203113003, 01203114201, 01203122501, 01203122502, 01203122503, 01203122504, 01203122601, 01203122602, 01203122603, 01203122604, 01216015501, 01216046301, 01226258801, 01236449801, 01236452801, 01246647401, 01246652801 and 177 more |
| Model numbers | 360030-1C, 360030-1CE, 360030-1CT, 360030-1CTS, 360030-XC, 360030-XCE, 360030-XCT, 360030-XCTS, 3600301-CTS, 36030-XCT |
Product
Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 360030-1CTS, 360030-XCTS, 3600301-CTS, 360030-XCE, 360030-1CT, 360030-1CE, 36030-XCT
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-1503-2026. 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.