Medline recalls PVC laryngeal masks with risk of cuff disconnecting from breathing tube. Affected units include specific model numbers and lots. Stop using if you have these items.
The mask cuff may disconnect from the device's breathing tube.
Medline is recalling PVC laryngeal masks that may disconnect the mask cuff from the breathing tube. This could lead to breathing difficulties during medical procedures. Owners should check if their masks match the listed model numbers and lots.
The mask cuff may disconnect from the breathing tube during use, potentially causing breathing difficulties. This could happen if the mask is not properly secured or if the cuff becomes loose. The risk is highest during medical procedures where the mask is used.
Healthcare professionals and medical facilities using Medline Standard PVC Laryngeal Masks are most at risk. Patients during procedures could be affected if the mask disconnects.
Check for Medline Standard PVC Laryngeal Masks with model numbers DYND290010 through DYND290050 and specific lots listed in the recall notice. The product comes in pouches with 5 masks per box.
Look for model numbers DYND290010 through DYND290050 and the listed lots to confirm if your masks are affected.
If your masks match the recalled model numbers and lots, stop using them immediately to prevent breathing issues during procedures.
The affected model numbers are DYND290010 through DYND290050 with specific lots listed in the recall notice.
Check the model number and lot numbers on your mask. Affected masks have model numbers DYND290010 through DYND290050 and the specific lots listed in the recall notice.
The recall does not specify a return process, but you should stop using affected masks immediately.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0941-2022 — Medline Medline Hello, I own a Medline that is covered by recall Z-0941-2022 from Medline. 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.
