Penner Pacific Bathing Spa, Model Numbers 360020-1P
FDA device recall Z-1502-2026 · posted 2026-03-09 · Open, Classified
Recall details
- Recalling firm
- Penner Patient Care, Inc.
- Reason for recall
- The device does not bear a unique device identifier.
- Action taken
- Recall notification letters were sent to customers beginning 8/13/25. Your facility has been identified as one that has purchased a Penner Bathing Spa and must place the label(s) attached to this letter(s) next to the current serial tag on your existing Penner Spa and, if applicable, Penner Reservoir. The existing serial tags are located on the side of the spa or reservoir. The serial tag is located behind the TV if you have a Penner Premier Spa with a TV in the cabinet. The last 11 numbers on the UDI label should match the serial number of your existing Penner Spa or Penner Reservoir. Please make sure you attach the corresponding UDI label to the correct Penner product. If you have any questions, please don t hesitate to call our office at 1-800-732-0717.
- Root cause
- Error in labeling
- Status
- Open, Classified
- Product code
- ILJ
- Quantity affected
- 45 units
- Distribution
- US Nationwide distribution.
- Date initiated
- 2025-08-13
- Date posted
- 2026-03-09
- Location
- Aurora, NE
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEM (K040772) | Penner Manufacturing, Inc. | 2004-04-05 |