Penner recalls Pacific Bathing Spas with specific model numbers 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 specific models of Pacific Bathing Spas because they do not have a unique device identifier. This issue means the product cannot be properly tracked or regulated, but it does not pose an immediate safety risk.
The device does not bear a unique device identifier, which is required for regulatory tracking and safety compliance. This means the product cannot be properly monitored for safety issues or recalls, but it does not cause immediate physical harm.
Owners of Penner Pacific Bathing Spas with model numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, and other listed models are affected. People using these spas for personal care are most at risk due to the lack of unique identification.
Check if your Pacific Bathing Spa has model numbers listed in the recall notice, such as 360030-1C, 360030-1CE, or 360030-1CTS. Also, verify the serial numbers provided in the recall list, which include numbers like 02216037601.
Identify your Pacific Bathing Spa's model number to see if it matches the recalled list.
Check the serial number on your product against the list of numbers provided in the recall notice.
The product does not bear a unique device identifier, which is required for regulatory tracking and safety compliance.
Check your model number against the list of recalled models (e.g., 360030-1C, 360030-1CE) and verify the serial number against the provided list.
The recall does not require immediate action beyond checking if your product is affected. No specific remedy is provided.
We’ve drafted a message you can send Penner to request your refund or repair — edit it as you like.
Subject: Recall Z-1503-2026 — Penner Penner Hello, I own a Penner that is covered by recall Z-1503-2026 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.
