medical LOW RISK Updated 2026-03-18

Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X

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Recalled Product

Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2

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Hazard / Issue

The device does not bear a unique device identifier.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 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

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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