Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Low |
| Status | ongoing |
| Recall date | August 13, 2025 |
| Reported | March 18, 2026 |
| Recalling firm | Penner Patient Care, Inc. |
| Country / region | United States NE |
Hazard
The device does not bear a unique device identifier.
Affected products
- Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X
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