FDA Device recall Z-1507-2026
Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1
- 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 760010-1, 770010-1 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-1507-2026 |
| 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 760010-1, 770010-1
Reason
The device does not bear a unique device identifier.
Identifiers
| code_info | UDI-DI: 0085007365408; Serial Numbers: 08216172001 07205587101 09195387501 06216130401 06226336703 03226285001 07205587…UDI-DI: 0085007365408; Serial Numbers: 08216172001 07205587101 09195387501 06216130401 06226336703 03226285001 07205587102 07205587102 10216194401 05205566901 08205620801 08246753903 06226345801 05216107103 08216170401 08195374901 09205629101 02226268801 05216098901 05246710101 04226317301 01226251403 08195367701 02226274601 08195367501 11226430901 10246773202 10246778301 02205500703 12195458301 03226297101 10205654401 10205654402 10246773201 01236457201 10195408001 05216106401 11216217002 06226336702 02256885901 10246776501 01205470801 02205500701 02216027601 09195396901 02236474901 02216042601 06246726801 01205470701 01236457202 02226268802 04216087001 03236497001 02246658801 07205601501 09216184102 10205654302 11216217001 04205552801 08195374801 03205534001 05205553001 05205553002 07205605501 07205605502 07205605503 07205605504 07205605505 02226278501 03236482501 01246639801 01246651201 01246651202 11236614902 08195367801 01226251401 09205628801 06216115102 09216184103 08246752402 1 |
|---|
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-1507-2026%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.