Penner recalls Pacific Bathing Spas with model numbers 350010-1, 350000-2, and 350010-X due to lack of a 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 products cannot be properly tracked or regulated, which could lead to safety risks if the device is used without proper identification.
The device does not have a unique device identifier, which is required for tracking and regulatory compliance. Without this identifier, the product cannot be properly monitored for safety issues or recalls, potentially leading to unaddressed risks.
Owners of Penner Pacific Bathing Spas with model numbers 350010-1, 350000-2, or 350010-X are affected. Those who use these spas for medical care are at higher risk due to the lack of device identification.
Check if your Pacific Bathing Spa has model numbers 350010-1, 350000-2, or 350010-X. The recall includes specific serial numbers listed in the official notice.
Identify your Pacific Bathing Spa model number to see if it matches 350010-1, 350000-2, or 350010-X.
The recall is due to the device not bearing a unique device identifier, which is required for regulatory tracking and safety monitoring.
Check your model number against the listed numbers. If it matches, you may need to contact Penner for further instructions.
The recall does not specify a direct safety hazard, but the lack of a unique identifier could lead to unaddressed risks if the product is used without proper tracking.
We’ve drafted a message you can send Penner to request your refund or repair — edit it as you like.
Subject: Recall Z-1499-2026 — Penner Penner Hello, I own a Penner that is covered by recall Z-1499-2026 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.
