FDA Medical Device Recalls (openFDA)
Penner Patient Care, Inc.: Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
- Recall number
- Z-1505-2026
- Recalling firm
- Penner Patient Care, Inc.
- Product
- Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
- Status
- Open, Classified
- Initiated
- 2025-08-13
- Posted
- 2026-03-09
- Terminated
- not on file
- Reason
- The device does not bear a unique device identifier.
- Root cause
- Error in labeling
- Action
- 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.
- Quantity
- 25 units
- Distribution
- US Nationwide distribution.
- Lot, serial or model codes
- UDI-DI: 0085007365406; Serial Numbers: 11185169701 01205459101 09236589001 08226376601 05236519007 07154096101 09185123501 09205645001 06216123501 06216123502 06216123503 04246695301 05205559701 05226325001 05226333501 03216074601 03216074602 03216074603 03216074604 04195277301 04216084201 05246707001 06195314201 03256918201 03256945401
- 510(k) numbers
- ["K040772"]
- PMA numbers
- not on file
- Product code
- ILJ
- Firm FEI
- 1922538
- Firm city
- Aurora
- Firm state
- NE
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28