Penner recalls Pacific Bathing Spas with model 360020-1EP due to lack of unique device identifier. Affected units may not be properly tracked for safety.
The device does not bear a unique device identifier.
Penner is recalling Pacific Bathing Spas with model number 360020-1EP because they do not have a unique device identifier. This means the product cannot be properly tracked for safety reasons.
The device lacks a unique identifier, which prevents it from being properly tracked and monitored for safety. Without this identifier, the product cannot be verified for compliance with safety standards.
Owners of Pacific Bathing Spas with model number 360020-1EP are affected. People using these spas for medical care may be at higher risk due to the lack of tracking.
Check for model number 360020-1EP on the product. The unique device identifier (UDI-DI) is listed as 0085007365402 on the recall notice.
Look for the model number 360020-1EP and the unique device identifier (UDI-DI) 0085007365402 on the product.
The product lacks a unique device identifier, which prevents it from being properly tracked for safety reasons.
Check for model number 360020-1EP and the unique device identifier (UDI-DI) 0085007365402 on the product.
The recall notice does not specify a remedy, so no action is required beyond checking if your product matches the model and identifier.
We’ve drafted a message you can send Penner to request your refund or repair — edit it as you like.
Subject: Recall Z-1501-2026 — Penner Penner Hello, I own a Penner that is covered by recall Z-1501-2026 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.
