Penner recalls Pacific Bathing Spas with model numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL due to missing unique device identifier. Consumers should check serial numbers listed in the recall notice.
The device does not bear a unique device identifier.
Penner is recalling Pacific Bathing Spas with specific model numbers because they lack a unique device identifier. This issue means the product cannot be properly tracked or regulated, which could lead to safety concerns if the device is not correctly identified.
The device does not have a unique device identifier (UDI-DI), which is required for tracking and regulatory compliance. Without this identifier, the product cannot be properly monitored for safety issues or recalls. This could lead to potential safety risks if the device is not correctly identified during use or maintenance.
Owners of Penner Pacific Bathing Spas with model numbers 560010-2L, 560010-XL, 560010-1L, or 560010-XL are affected. Individuals using these spas for medical care may be at higher risk due to the missing identifier.
Check the model numbers on your Penner Pacific Bathing Spa: 560010-2L, 560010-XL, 560010-1L, or 560010-XL. Also, verify the serial numbers listed in the recall notice, which include specific numbers like 11154213601 and others.
Identify if your spa has model numbers 560010-2L, 560010-XL, 560010-1L, or 560010-XL.
Compare your spa's serial number with the list provided in the recall notice.
The recall is due to the device not bearing a unique device identifier (UDI-DI), which is required for regulatory tracking and safety compliance.
The recall does not require immediate discontinuation of use; however, you should check if your spa is affected and verify the serial numbers.
Check the model numbers and serial numbers listed in the recall notice to see if they match the affected units.
We’ve drafted a message you can send Penner to request your refund or repair — edit it as you like.
Subject: Recall Z-1506-2026 — Penner Penner Hello, I own a Penner that is covered by recall Z-1506-2026 from Penner. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
