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

Penner Patient Care, Inc.: Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X

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: 21 units Lot/code info: UDI-DI: 0085007365400; Serial Numbers: 06020315401 08010223607 04205543401 05246707501 05246707502 02195222101 11216213301 09185118801 10216206001 10216206002 11216222201 11216222202 05246717201 02195236901 11195422801 01246647601 01246656501 04205544901 12205685701 09236590301 11195432401

UPC codes

0085007365400, 06020315401, 08010223607, 04205543401, 05246707501, 05246707502, 02195222101, 11216213301, 09185118801, 10216206001, 10216206002, 11216222201, 11216222202, 05246717201, 02195236901, 11195422801, 01246647601, 01246656501, 04205544901, 12205685701, 09236590301, 11195432401

Source

Official record: FDA (Device enforcement)

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

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