Westmed recalls adult CO2/O2 masks with potential loose tubing connections that could delay oxygen treatment. Affected models include REF 0930 with specific dimensions and lot numbers.
There is a potential that the fitment between the oxygen delivery tube and the mask adapter may become loose. This could result in the device tubing not making a secure connection to the mask adapter resulting in a possible delay in treatment.
Westmed is recalling adult CO2/O2 masks that may have loose connections between the oxygen tube and mask adapter. This could delay critical oxygen treatment for patients. Users should check if their mask matches the described model and lot number.
The oxygen delivery tube might become loose in the mask adapter, causing a delay in oxygen delivery. This could be critical for patients needing immediate treatment.
Patients using this mask for oxygen therapy are most at risk. The recall affects specific models sold with particular lot numbers.
Check for the model REF 0930 with 7' tubing, Sivel GSE, 10' GSL, and reflective features. The lot number 091620N04 is also associated with this recall.
Verify your mask has the model REF 0930 with 7' tubing, Sivel GSE, 10' GSL, and reflective features.
The mask may have a loose connection between the oxygen tube and mask adapter, which could delay oxygen treatment.
Check if your mask matches the model and lot number described in the recall. If it does, contact Westmed for further instructions.
The recall indicates a potential risk of delayed treatment, so users should check if their mask is affected before continuing use.
We’ve drafted a message you can send Westmed to request your refund or repair — edit it as you like.
Subject: Recall Z-0743-2021 — Westmed Westmed Hello, I own a Westmed that is covered by recall Z-0743-2021 from Westmed. 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.
