Penner recalls Pacific Bathing Spas with model numbers 390010-1, 390010-X, 390010-2 due to lack of 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 do not have a unique device identifier. This issue means the product cannot be tracked or verified for safety compliance, but it does not pose an immediate physical risk.
The device lacks a unique device identifier, which is required for tracking and verifying safety compliance. Without this identifier, the product cannot be properly monitored for potential safety issues. However, this does not cause immediate physical harm.
Owners of Pacific Bathing Spas with model numbers 390010-1, 390010-X, or 390010-2 are affected. People using these spas for medical care are most at risk due to the lack of tracking for safety compliance.
Check if your Pacific Bathing Spa has model numbers 390010-1, 390010-X, or 390010-2. The recall includes specific serial numbers listed in the official notice.
Identify if your Pacific Bathing Spa has model numbers 390010-1, 390010-X, or 390010-2.
The product lacks a unique device identifier, which is required for tracking and verifying safety compliance.
No, the recall does not require stopping use. The issue is about missing identification, not immediate safety risks.
Check if your Pacific Bathing Spa has model numbers 390010-1, 390010-X, or 390010-2, and verify the serial numbers listed in the recall notice.
We’ve drafted a message you can send Penner to request your refund or repair — edit it as you like.
Subject: Recall Z-1505-2026 — Penner Penner Hello, I own a Penner that is covered by recall Z-1505-2026 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.
