Drug recall
Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
FDA recall event 98396 · Class III · Penner Patient Care, Inc.
Key facts
| Event ID | 98396 |
|---|---|
| Recall numbers | Z-1499-2026, Z-1500-2026, Z-1501-2026, Z-1502-2026, Z-1503-2026, Z-1504-2026, Z-1505-2026, Z-1506-2026, Z-1507-2026, Z-1508-2026 |
| Recalling firm | Penner Patient Care, Inc. |
| Product type | Devices |
| Products | Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X, 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…, Penner Pacific Bathing Spa, Model Numbers 360020-1EP, Penner Pacific Bathing Spa, Model Numbers 360020-1P, 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… and 5 more |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The device does not bear a unique device identifier. |
| Initiation date | Aug 13, 2025 |
| Report date | Mar 18, 2026 |
| City | Aurora |
| State | NE |
| Country | United States |
| FEI number | 1922538 |
At a glance
- 10–99 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: