Gibeck Humid-Vent 2S Flex DC humidifiers with specific product numbers (17731, 17732, 19061, 19062, 19812) have reported torn corrugated breathing tubes. Consumers should check their product numbers against the list provided.
Reports received of torn corrugated breathing tubes.
Gibeck Humid-Vent 2S Flex DC humidifiers with product numbers 17731, 17732, 19061, 19062, and 19812 have been recalled due to reports of torn corrugated breathing tubes. This could lead to breathing difficulties if the tube is damaged.
Torn corrugated breathing tubes can cause breathing difficulties if the tube is damaged. The tubes are part of the humidifier system that delivers moisture to the air.
Users of Gibeck Humid-Vent 2S Flex DC humidifiers with the listed product numbers are affected. Those with the specific product numbers mentioned in the recall are most at risk.
Check your Gibeck Humid-Vent 2S Flex DC humidifier's product number against the list: 17731 (sterile), 17732 (non-sterile), 19061 (sterile), 19062 (non-sterile), and 19812 (non-sterile).
Compare your humidifier's product number to the list of affected numbers: 17731, 17732, 19061, 19062, or 19812.
The recall is due to reports of torn corrugated breathing tubes, which could cause breathing difficulties.
Check your product number against the list: 17731 (sterile), 17732 (non-sterile), 19061 (sterile), 19062 (non-sterile), or 19812 (non-sterile).
Check your product number against the list provided in the recall. If affected, contact the manufacturer for further instructions.
We’ve drafted a message you can send Gibeck to request your refund or repair — edit it as you like.
Subject: Recall Z-1126-2022 — Gibeck Gibeck Hello, I own a Gibeck that is covered by recall Z-1126-2022 from Gibeck. 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.
