FDA DevicesClass III
Penner Pacific Bathing Spa, Model Numbers 360020-1EP
Published: March 18, 2026Recall ID: Z-1501-2026Category: devicesCountry: US
Reason for Recall / Hazard
The device does not bear a unique device identifier.
Product Description & Identification
Penner Pacific Bathing Spa, Model Numbers 360020-1EP
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: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803 |
| Postal code | 68818-3200 |
| Report date | 20260318 |
| Product type | Devices |
| Product quantity | 10 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.