FDA DevicesClass III
Penner Pacific Bathing Spa, Model Numbers 360020-1P
Published: March 18, 2026Recall ID: Z-1502-2026Category: devicesCountry: US
Reason for Recall / Hazard
The device does not bear a unique device identifier.
Product Description & Identification
Penner Pacific Bathing Spa, Model Numbers 360020-1P
Additional Source Details
| Field | Value |
|---|---|
| City | Aurora |
| State | NE |
| Event id | 98396 |
| Address 1 | 101 Grant St |
| Address 2 | N/A |
| Code info | UDI-DI: 0085007365403; Serial Numbers: 11193097601 10216195501 10216195502 12193104901 06226342101 06226342102 06226342105 06226342107 03203148701 01226259601 10226410801 06246724701 10203210401 10203210402 05216113101 11193095401 01203118301 05216107301 05216107302 05216107303 05216107304 05216107305 05216108301 05216108302 06193030201 03203147601 09193066601 03216060801 07193052301 09236591501 02246673801 02192976301 03246682701 01192960801 01192960802 06236535501 08152390701 03216065101 05182864901 01142094001 11121856201 03192998301 01192959801 01226256901 03256938801 |
| Postal code | 68818-3200 |
| Report date | 20260318 |
| Product type | Devices |
| Product quantity | 45 units |
| Reason for recall | The device does not bear a unique device identifier. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20250813 |
| Initial firm notification | Letter |
| Center classification date | 20260309 |
Overview
- Recalling FirmPenner Patient Care, Inc.
- StatusOngoing
- Risk LevelClass III
- DistributionUS Nationwide distribution.