FDA Device recall Z-1501-2026
Penner Pacific Bathing Spa, Model Numbers 360020-1EP
- FDA Device
- Class III
- ongoing
- Published 2026-03-18
On 2026-03-18 the FDA classified a Class III recall of Penner Pacific Bathing Spa, Model Numbers 360020-1EP by Penner Patient Care, citing the device does not bear a unique device identifier.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1501-2026 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2025-08-13 |
| Published | 2026-03-18 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Penner Patient Care |
| Distribution | US |
Product
Penner Pacific Bathing Spa, Model Numbers 360020-1EP
Reason
The device does not bear a unique device identifier.
Identifiers
| code_info | UDI-DI: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1501-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.