FDA-Device2026-03-18Class IIIMISBRANDING

Penner Pacific Bathing Spa recalled for missing unique device identifier

OTHERNationwide distribution

Check your Penner Pacific Bathing Spa serial number

Certain Penner Pacific Bathing Spa models do not have a unique device identifier (UDI) as required by federal regulations. This affects 643 units with specific serial numbers. No injuries have been reported.

  • Check if your bathing spa serial number matches the FDA recall list
  • Contact Penner Patient Care, Inc. for instructions on next steps
  • Do not discard the device until you receive guidance from the manufacturer
Hazard

The device does not bear a unique device identifier.

Sold states
US Nationwide distribution.
Affected count
643 units
Manufactured in
101 Grant St, N/A, Aurora, NE, United States
Products
Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-2WL, 360010-X, 370000-XW, 360010-2W, 362010-2, 360010, 37000-XWL, 362010-X, 362010-XL, 362010-1L, 360010-XL, 37000-1W, 360010-XW, 3700000-1W, 362010-2L, 36010-XWT, 370000-1L, 360010-2WT, 360000-1, 360010-XWSB, 360010-XLSB

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1500-2026

More Penner Patient Care, Inc. recalls

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief