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FDA (Device enforcement)Recalled 2025-08-13class iii

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

Hazard

The device does not bear a unique device identifier.

Details from the source

Reason for recall: The device does not bear a unique device identifier. Distribution: US Nationwide distribution. Quantity: 26 units 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

UPC codes

0085007365409, 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

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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