Penner recalls Pacific Bathing Spas with specific model numbers due to lack of unique device identifier. Consumers should check serial numbers and contact Penner for details.
The device does not bear a unique device identifier.
Penner is recalling Pacific Bathing Spas with certain model numbers 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 lacks a unique device identifier, which is required for tracking and regulatory compliance. This means the product cannot be properly monitored for safety or quality issues, but it does not cause immediate harm.
Owners of Pacific Bathing Spas with model numbers listed in the recall (e.g., 361910-1A) are affected. Most at risk are users who may not be aware of the missing identifier.
Check the model numbers listed in the recall (e.g., 361910-1A) and serial numbers provided. The product is sold by Penner Patient Care, Inc.
Look for model numbers like 361910-1A on the product label.
Reach out to Penner Patient Care, Inc. for further assistance with the recall.
The product lacks a unique device identifier, which is required for regulatory tracking but does not pose an immediate safety risk.
No, the recall does not require stopping use; it is a regulatory issue, not a safety hazard.
Check the model numbers and 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-1504-2026 — Penner Penner Hello, I own a Penner that is covered by recall Z-1504-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.