[Recalled] 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 — The device does not bear a unique device identifier | FDA 2025-08-1
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | 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 |
|---|---|
| Brand / manufacturer | Penner Patient Care, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1504-2026 |
| Country of notice | United States |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 13 August 2025 |
| EAN / barcode | 0085007365405 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The device does not bear a unique device identifier.
This Class III recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Penner Patient Care, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.