medical LOW RISK Updated 2026-03-18

Penner Patient Care, Inc. recalls Penner Pacific Bathing Spa, Model Numbers 860010-1L

See all recalls from Penner Patient Care, Inc. →

Recalled Product

Penner Pacific Bathing Spa, Model Numbers 860010-1L

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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: 0085007365409; Serial Numbers: 07246737902 10236603401 10226407101 03236488101 03246677601 08226379901 08226385601 12236632601 07226353601 08236572201 04246696501 01256844001 12246811601 06226337201 07236557301 09236582001 02246663101 09246761901 08226369401 08226374601 01246644601 04246691701 08246756001 10236600001 04256958001 04256952001

✅ 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.

Looking for a safe alternative?

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View official government recall

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