medical LOW RISK Updated 2026-03-18

Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa, Model Numbers 360020-1EP

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Recalled Product

Penner Pacific Bathing Spa, Model Numbers 360020-1EP

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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: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803

✅ 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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View official government recall

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