Penner Patient Care recalled 10 Penner Pacific Bathing Spa units nationwide on 2025-08-13 after regulators flagged the device lacks a unique device identifier. The device does not bear a unique device identifier. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.
The device does not bear a unique device identifier.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Penner Patient Care, Inc. or your healthcare provider for instructions. Notification method: Letter
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The Penner Pacific Bathing Spa is a medical device used for patient bathing. It is distributed nationwide and part of home or clinical care settings.
The device lacks a unique device identifier, which can impede product tracking and safety recalls. It does not imply an immediate personal injury by itself but raises regulatory and safety-tracking concerns.
This recall is not part of a broader industry pattern.
Consumers must stop using the device and await instructions. The missing UDI could complicate adverse event reporting and product recalls.
Look on the device label for model, UDI-DI, and serial numbers. The recall notice provides the identifiers.
Remedies such as refunds or replacements can take 4-8 weeks.
Document serial numbers, model, and purchase details. Save recall notices and correspondence with the manufacturer.
Model numbers: 360020-1EP. UDI-DI: 0085007365402. Serial Numbers: 03203147501, 01192957001, 06203171301, 07203175701, 11162597701, 11193074801, 11193074802, 09193074801, 09193074802, 09193074803. Quantity: 10 units. Sold nationwide in the United States. Recall date: 2025-08-13. Manufacturer: Penner Patient Care, Inc. Status: Active.
No injuries or incidents have been reported.
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