Penner Patient Care

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa units (Model 860010-1L) because they do not have the required unique device identifier marked on them. This identifier is needed for proper tracking and safety oversight. No injuries have been reported.

Certain Penner Pacific Bathing Spa units (Models 760010-1 and 770010-1) were distributed without a required unique device identifier (UDI) label. This label helps health authorities track and manage medical devices. The FDA has identified 190 affected units by serial number.

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa models because they do not have the required unique device identifier (UDI) label. This makes it difficult to track the device for safety purposes. No injuries have been reported.

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa models (390010-1, 390010-X, 390010-2) because they do not have the required unique device identifier. This is a regulatory compliance issue. About 25 units are affected.

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa units because they do not have the required unique device identifier (UDI) label. This is a regulatory compliance issue. No injuries have been reported.

Certain Penner Pacific Bathing Spa models do not have a unique device identifier (UDI) as required by FDA regulations. This affects 206 units with specific serial numbers distributed nationwide. No injuries have been reported.

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa units (Model 360020-1P) because they do not have a unique device identifier (UDI) as required by federal regulations. This affects 45 units distributed nationwide. No injuries have been reported.

The device does not bear a unique device identifier.

Certain Penner Pacific Bathing Spa models do not have a unique device identifier (UDI) as required by federal regulations. This affects 643 units with specific serial numbers. No injuries have been reported.

Penner Patient Care is recalling certain Penner Pacific Bathing Spa models because they do not have the required unique device identifier marked on them. This identifier helps track and manage the device if problems arise. No injuries have been reported.