Bathing Spa Recall: Penner Pacific 360020-1P
Announced 2026-03-18 · FDA
FDA recalls Penner Pacific Bathing Spa devices because the units do not bear a unique device identifier. The recall involves 25 units distributed nationwide in the US and includes UDI-DI 0085007365406 with a listed set of serial numbers. The provided information does not specify a corrective action, and the recall is categorized as low severity.
| Brand | Penner Patient Care, Inc. |
|---|---|
| Product | Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2 |
| Reason | The device does not bear a unique device identifier. |
| Severity | low |
| Units affected | 45 |
| Distribution | US Nationwide distribution. |
| Agency | FDA |
| Recall / campaign no. | UDI-DI: 0085007365406; Serial Numbers: 11185169701 01205459101 09236589001 08226376601 05236519007 07154096101 09185123501 09205645001 06216123501 06216123502 06216123503 04246695301 05205559701 05226325001 05226333501 03216074601 03216074602 03216074603 03216074604 04195277301 04216084201 05246707001 06195314201 03256918201 03256945401 |
WHAT YOU SHOULD DO
- Stop using the recalled device immediately.
- Check if your unit matches the listed UDI-DI 0085007365406 or any of the serial numbers to confirm eligibility.
- Contact Penner Patient Care, Inc. for instructions regarding remedy or replacement.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.