Class III — Penner Patient Care, Inc.
| Recalling firm | Penner Patient Care, INC |
|---|---|
| Registered facility | Penner Patient Care, INC (the firm's only registered facility) |
| Classification | Class III |
| Status | Ongoing |
| Reason | The device does not bear a unique device identifier. |
| 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 |
| Quantity | 643 units |
| Distribution | US Nationwide distribution. |
| Initiated | 2025-08-13 |
| Classified | 2026-03-09 |
| Recall number | Z-1500-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class III recall — Penner Patient Care, Inc. (Z-1500-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98396/
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